(406 days)
No
The device description and intended use are for bone plates and screws, which are mechanical implants. There is no mention of software, algorithms, or any technology that would incorporate AI/ML.
Yes
The device, consisting of various bone plates and screws, is intended for treating fractures, non-unions, and osteotomies of bones like the humerus and ulna, which are conditions requiring therapeutic intervention to mend bone injuries and restore function.
No
This device is described as a system of bone plates and screws for surgical implantation to treat fractures, which is a therapeutic function, not a diagnostic one.
No
The device description clearly states that the system consists of "various types of bone plates, Screws for implantation" and describes physical components like "medial and postero-lateral distal humerus plates" and "locking compression holes." This indicates a hardware-based medical device, not a software-only one.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use/Indications for Use: The intended use clearly describes the device as bone plates and screws for treating fractures and non-unions of the humerus, ulna, radius, tibia, and fibula. This is a surgical implant used directly on the patient's bone.
- Device Description: The description further confirms that the device consists of bone plates and screws for implantation in bone.
- IVD Definition: An In Vitro Diagnostic device is used to examine specimens derived from the human body (like blood, urine, tissue) to provide information for diagnosis, monitoring, or screening. This device does not interact with such specimens.
The device described is a surgical implant used for orthopedic fixation.
N/A
Intended Use / Indications for Use
Specific Indications:
-
- 2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate
2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate is intended for treating of Intraarticular Fracture of the distal humerus, Supracondylar fractures of the distal humerus and Non-unions of the distal humerus.
- 2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate
- 2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate with Lateral Support
2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate with Lateral Support is intended for treating of Intraarticular fractures of the distal humerus, Supracondylar fractures of the distal humerus and Non-unions of the distal humerus.
- 2.7/3.5mm Wise-Lock Dorsolateral Medial Distal Humerus Plate
2.7/3.5mm Wise-Lock Dorsolateral Medial Distal Humerus Plate are indicated for treating of Intraarticular fractures of the distal humerus, Supracondylar fractures of the distal humerus and Non-unions of the distal humerus.
- 3.5mm Wise-Lock Extra-Articular Distal Humerus Plate
3.5mm Wise-Lock Extra-Articular Distal Humerus Plate are indicated for fractures of the distal humerus.
- PHEELOS-3.5mm Wise-Lock Proximal Humerus Plate, Short
PHEELOS Short Indications
- · Dislocated two-, three-, and four-fragment fractures of the proximal humerus
- · Pseudarthroses in the proximal humerus
- · Osteotomies in the proximal humerus
- PHEELOS-3.5mm Wise-Lock Proximal Humerus Plate, Long
• As for PHEELOS Short, but for fractures extending to the shaft or without medial support.
- 3.5mm Wise-Lock Proximal Humerus Plate
The 3.5mm Wise-Lock Proximal Humerus Plate is intended for fractures and fracture dislocations, and nonunions of the proximal humerus.3
- 3.5mm Wise-Lock Periarticular Proximal Humerus Plate
3.5mm Wise-Lock Periarticular Proximal Humerus Plate are indicated for fracture dislocations, osteotomies, and nonunions of the proximal humerus.
- 3.5mm Wise-Lock Olecranon Plate
3.5mm Wise-Lock Olecranon Plate is indicated for fixation of fractures and non-unions of the olecranon.
- 3.5mm Wise-Lock Hook Plate
3.5mm Wise-Lock Hook Plate is indicated for fractures, osteotomies of small bones including the ulna, radius, tibia and fibula.
- 2.7mm Wise-Lock Screw, Self-Tapping (Hex Head)
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
- 3.5mm Wise-Lock Screw, Self-Tapping (Hex Head)
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
- 3.5mm Wise-Lock Screw, Self-Drilling, (Hex Head)
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
-
3.5mm Wise-Lock Cancellous Screw, Full Thread, Self-Tapping, (Hex Head) This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
-
3.5mm Wise-Lock Cancellous Screw, Short Thread, Self-Tapping, (Hex Head) This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
-
3.5mm Cortical Screw, Self-Tapping, (Hex Head)
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
- 4.0mm Cancellous Screw, Short Thread
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
- 4.0mm Cancellous Screw, Full Thread
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
- 2.7mm Cortical Screw, Self-Tapping, (Hex Head)
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
Product codes (comma separated list FDA assigned to the subject device)
HRS, HWC
Device Description
The Humerus and Ulna System consists of various types of bone plates, Screws for implantation in the humerus and ulna bone to treat humerus and ulna bone fractures.
The Humerus and Ulna System consists of medial and postero-lateral distal humerus plates of various lengths and 2.7 mm locking screws. The plates are pre-contoured to match the anatomy of the distal humerus with a limited contact low profile design. The plate features locking compression holes which accept 2.4, 3.5, & 4.0 mm cortex screws, 2.4, 2.7 & 3.5 mm locking screws, and 4.0 mm cancellous screws. The System is available in Stainless Steel and Titanium.
These implants are sold in both non-sterile and sterile conditions.
Note- Non sterile products have to be sterilized before use.
The system is indicated for use in adult patients only. All implants are for single use only.
The humerus and Ulna System contains several plates and each plate has its intended uses. The intended uses for all plates are given below:
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Humerus, Ulna, Radius, Tibia, Fibula
Indicated Patient Age Range
Adult patients only.
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Bench tests were conducted to verify that the subject device met all design specifications. The test results demonstrated that the subject device complies with the following standards: Material Standards (ASTM F136/ISO 5832-3, ASTM F899-12, ASTM F138/ISO 5832-1), Biocompatibility (ISO 10993), Mechanical performance (ASTM F382 (Metallic Bone Plates) and ASTM F543 (Metallic Medical Bone Screws)), Sterilization, shelf-life and packaging for sterile product (ISO 11137-1, ISO 11137-2, ISO 11137-3, ISO 17665-1, ISO/TS 17665-2, ISO/TS 17665-3, ISO 11140-1, ISO 11737-1, ISO 11737-2, ISO 11607-1/AMD1, ISO 11607-2/AMD1, ASTM F1980, ASTM F88/F88M, ASTM F1929), and Bacterial Endotoxin (USP , USP ).
Key results: The results of this testing indicate that the Humerus and Ulna System is equivalent to the predicate device.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 888.3030 Single/multiple component metallic bone fixation appliances and accessories.
(a)
Identification. Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.(b)
Classification. Class II.
0
November 4, 2022
Auxein Medical Private Limited Rahul Luthra Director Plot No. 168, 169, 170 Phase-IV, Sector 57, Kundli Industrial area Sonipat, Haryana 131028 India
Re: K213108
Trade/Device Name: Humerus & Ulna System Regulation Number: 21 CFR 888.3030 Regulation Name: Single/Multiple Component Metallic Bone Fixation Appliances And Accessories Regulatory Class: Class II Product Code: HRS, HWC Dated: October 5, 2022 Received: October 5, 2022
Dear Rahul Luthra:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
1
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely.
Shumaya Ali-S
Shumaya Ali, M.P.H. Assistant Director DHT6C: Division of Restorative, Repair and Trauma Devices OHT6: Office of Orthopedic Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
2
Indications for Use
510(k) Number (if known) K213108
Device Name Humerus and Ulna System
Indications for Use (Describe)
Specific Indications:
-
- 2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate
2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate is intended for treating of Intraarticular Fracture of the distal humerus, Supracondylar fractures of the distal humerus and Non-unions of the distal humerus.
- 2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate
- 2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate with Lateral Support
2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate with Lateral Support is intended for treating of Intraarticular fractures of the distal humerus, Supracondylar fractures of the distal humerus and Non-unions of the distal humerus.
- 2.7/3.5mm Wise-Lock Dorsolateral Medial Distal Humerus Plate
2.7/3.5mm Wise-Lock Dorsolateral Medial Distal Humerus Plate are indicated for treating of Intraarticular fractures of the distal humerus, Supracondylar fractures of the distal humerus and Non-unions of the distal humerus.
- 3.5mm Wise-Lock Extra-Articular Distal Humerus Plate
3.5mm Wise-Lock Extra-Articular Distal Humerus Plate are indicated for fractures of the distal humerus.
- PHEELOS-3.5mm Wise-Lock Proximal Humerus Plate, Short
PHEELOS Short Indications
- · Dislocated two-, three-, and four-fragment fractures of the proximal humerus
- · Pseudarthroses in the proximal humerus
- · Osteotomies in the proximal humerus
- PHEELOS-3.5mm Wise-Lock Proximal Humerus Plate, Long
• As for PHEELOS Short, but for fractures extending to the shaft or without medial support.
- 3.5mm Wise-Lock Proximal Humerus Plate
The 3.5mm Wise-Lock Proximal Humerus Plate is intended for fractures and fracture dislocations, and nonunions of the proximal humerus.3
- 3.5mm Wise-Lock Periarticular Proximal Humerus Plate
3.5mm Wise-Lock Periarticular Proximal Humerus Plate are indicated for fracture dislocations, osteotomies, and nonunions of the proximal humerus.
- 3.5mm Wise-Lock Olecranon Plate
3.5mm Wise-Lock Olecranon Plate is indicated for fixation of fractures and non-unions of the olecranon.
- 3.5mm Wise-Lock Hook Plate
3.5mm Wise-Lock Hook Plate is indicated for fractures, osteotomies of small bones including the ulna, radius, tibia and fibula.
- 2.7mm Wise-Lock Screw, Self-Tapping (Hex Head)
3
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
- 3.5mm Wise-Lock Screw, Self-Tapping (Hex Head)
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
- 3.5mm Wise-Lock Screw, Self-Drilling, (Hex Head)
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
-
3.5mm Wise-Lock Cancellous Screw, Full Thread, Self-Tapping, (Hex Head) This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
-
3.5mm Wise-Lock Cancellous Screw, Short Thread, Self-Tapping, (Hex Head) This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
-
3.5mm Cortical Screw, Self-Tapping, (Hex Head)
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
- 4.0mm Cancellous Screw, Short Thread
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
- 4.0mm Cancellous Screw, Full Thread
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
- 2.7mm Cortical Screw, Self-Tapping, (Hex Head)
This Screw is indicated for the fixation of bone and plate to produce compression in bones which is required to mend a bone injury.
Type of Use (Select one or both, as applicable)
X Prescription Use (Part 21 CFR 801 Subpart D)
Over-The-Counter Use (21 CFR 801 Subpart C)
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Image /page/4/Picture/1 description: The image shows the logo for Auxein. The logo consists of a blue circle with a stylized letter "A" inside, followed by the word "Auxein" in blue, with a registered trademark symbol next to it. The logo is simple and modern, and the blue color gives it a sense of trust and reliability.
Section 6.0: 510k Summary
Pre Market Notification 510(k) Summary as required by section 807.92 General Company Information as required by 807.92 (a) A.1: The Submitter's Name, address, telephone number, a contact person, and the date the summary was prepared.
| Submitter's Name: | Auxein Medical Private Limited |
|---|---|
| Address: | Auxein Medical Private Limited |
| Plot No. 168-169-170, Phase-4, Kundli Industrial Area, HSIIDC, | |
| Sector-57, Sonepat-131028, Haryana, India | |
| Contact Person Name: | Mr. Rahul Luthra |
| Title: | Director |
| Email Id: | info@auxein.com |
| Phone Number: | +91 9560557733 |
| Dated: | 04.11.2022 |
Person Responsible for Regulatory Compliance
| Name: | Mr. Mohit Kumar |
|---|---|
| Title: | Sr. Research Engineer |
| Email Id: | m.kumar@auxein.com |
| Dated: | 04.11.2022 |
Throughout the submission of Humerus and Ulna System is covered under 510(k) Submission.
A.2: The name of the device, including the trade or proprietary name if applicable, the common or usual name, and the classification name, if known
Proprietary Name: Humerus and Ulna System
Common or Usual Name: Plate, Fixation, Bone (Primary) Screw Fixation, Bone
Classification Name:
Single/multiple component metallic bone fixation appliances and accessories (Primary) Smooth or threaded metallic bone fixation fastener
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Image /page/5/Picture/1 description: The image shows the logo for Auxein. The logo consists of a blue circle with a stylized letter "A" inside of it. To the right of the circle is the word "Auxein" in blue, with a registered trademark symbol next to it.
Product Code:
HRS (Primary) HWC
Device Class: II
Review Panel: Orthopedic
Regulation Number:
21 CFR 888.3030 (Primary) 21 CFR 888.3040
| Primary Product
| Code | Classification Name | Common Name | Regulation Number |
|---|---|---|---|
| HRS | Single/multiple | ||
| component metallic | |||
| bone fixation | |||
| appliances and | |||
| accessories | Plate, Fixation Bone | 21 CFR 888.3030 |
Variants/Types:
Humerus and Ulna Systems consist of the following Components:
| S.No. | Product Description |
|---|---|
| 1. | 2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate (3, 5, 7, 9, 14 Holes), Left and |
| Right | |
| 2. | 2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate with Lateral Support (3, 5, 7, 9, |
| 14 Holes), Left and Right | |
| 3. | 2.7/3.5mm Wise-Lock Dorsolateral Medial Distal Humerus Plate, (3, 5, 7, 9, 14 Holes), |
| Left and Right | |
| 4. | 3.5mm Wise-Lock Hook Plate, (3, 4, 5 Holes) |
| 5. | 3.5mm Wise-Lock Extra-Articular Distal Humerus Plate, (4, 6, 8, 10, 12, 14 Holes), Left |
| and Right | |
| 6. | 3.5mm Wise-Lock Olecranon Plate, (2, 4, 6, 8, 10, 12 Holes), Left and Right |
| 7. | PHEELOS-3.5mm Wise-Lock Proximal Humerus Plate, Short, (3, 4, 5 Holes) |
| 8. | PHEELOS-3.5mm Wise-Lock Proximal Humerus Plate, Long, (5, 6, 8, 10, 12 Holes) |
| 9. | 3.5mm Wise-Lock Periarticular Proximal Humerus Plate, (2, 3, 4, 5, 6, 8, 10, 12, 14 |
| Holes), Left and Right |
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Image /page/6/Picture/0 description: The image shows the logo for Auxein. The logo consists of a blue circle with a white "A" inside of it. To the right of the circle is the word "Auxein" in blue, with a small "®" symbol in the upper right corner.
K213108
| 10. | 3.5mm Wise-Lock Proximal Humerus Plate, (5, 6, 7, 8 Holes) |
|---|---|
| Screws | |
| 11. | 2.7mm Wise-Lock Screw, Self-Tapping (Hex Head), (10-60mm) Length |
| 12. | 3.5mm Wise-Lock Screw, Self-Tapping (Hex Head), (10-80mm) Length |
| 13. | 3.5mm Wise-Lock Screw, Self-Drilling, (Hex Head), (10-60mm) Length |
| 14. | 3.5mm Wise-Lock Cancellous Screw, Full Thread, Self-Tapping, (Hex Head), (10-60mm) Length |
| 15. | 3.5mm Wise-Lock Cancellous Screw, Short Thread, Self-Tapping, (Hex Head), (10-60mm) Length |
| 16. | 3.5mm Cortical Screw, Self-Tapping, (Hex Head), (10-90 mm) Length |
| 17. | 4.0mm Cancellous Screw, Short Thread, (12-60 mm) Length |
| 18. | 4.0mm Cancellous Screw, Full Thread, (12-60 mm) Length |
| 19. | 2.7mm Cortical Screw, Self-Tapping, (Hex Head), Titanium (6-30 mm) Length |
A.3) Identification of the Predicate Device:
Following are the predicate device 510(K) with which we are declaring substantial equivalence: The following is the range of variants covered with their corresponding predicate devices.
Primary Predicate:
| 510K Number | K082625 |
|---|---|
| Applicant | Synthes, USA |
| Common Name | Bone Fixation Plates |
| Device Name | 3.5mm LCP Periarticular Proximal Humerus Plates |
Other Predicate:
| 510K Number | K082807 |
|---|---|
| Applicant | Synthes, USA |
| Common Name | 3.5 /4.5 mm LCP System |
| Device Name | Synthes 3.5mm LCP Olecranon Plates |
Reference Device:
| 510K Number | K033995 |
|---|---|
| Applicant | Synthes, USA |
| Common Name | Bone Fixation Plates |
| Device Name | 3.5 mm LCP Distal Humerus System |
| 510K Number | K141680 |
|---|---|
| ------------- | --------- |
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Image /page/7/Picture/1 description: The image shows the logo for Auxein. The logo consists of a blue circle with a stylized "A" inside of it. To the right of the circle is the word "Auxein" in blue, with a registered trademark symbol next to it.
| Applicant | Auxein Medical Private Limited, India |
|---|---|
| Common Name | Bone Fixation Plates |
| Device Name | Auxein Bone Plates and Screws |
| 510K Number | K082072 |
|---|---|
| Applicant | Synthes, USA |
| Common Name | Bone Fixation Plates |
| Device Name | 3.5 mm LCP Hook Plate |
A.4) A description of the device that is the subject of the pre market notification submission, such as might be found in the labelling or promotional material for the device.
Device Description:
The Humerus and Ulna System consists of various types of bone plates, Screws for implantation in the humerus and ulna bone to treat humerus and ulna bone fractures.
The Humerus and Ulna System consists of medial and postero-lateral distal humerus plates of various lengths and 2.7 mm locking screws. The plates are pre-contoured to match the anatomy of the distal humerus with a limited contact low profile design. The plate features locking compression holes which accept 2.4, 3.5, & 4.0 mm cortex screws, 2.4, 2.7 & 3.5 mm locking screws, and 4.0 mm cancellous screws. The System is available in Stainless Steel and Titanium.
These implants are sold in both non-sterile and sterile conditions.
Note- Non sterile products have to be sterilized before use.
The system is indicated for use in adult patients only. All implants are for single use only.
The humerus and Ulna System contains several plates and each plate has its intended uses. The intended uses for all plates are given below:
A.5) Indications for Use:
2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate
2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate is intended for treating of Intraarticular Fracture of the distal humerus, Supracondylar fractures of the distal humerus and Non-unions of the distal humerus.
2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate with Lateral Support
2.7/3.5mm Wise-Lock Dorsolateral Distal Humerus Plate with Lateral Support is intended for treating of Intraarticular fractures of the distal humerus, Supracondylar fractures of the distal humerus and Non-unions of the distal humerus.
2.7/3.5mm Wise-Lock Dorsolateral Medial Distal Humerus Plate
2.7/3.5mm Wise-Lock Dorsolateral Medial Distal Humerus Plate are indicated for treating of Intraarticular fractures of the distal humerus, Supracondylar fractures of the distal humerus and Nonunions of the distal humerus.
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Image /page/8/Picture/1 description: The image shows the logo for Auxein. The logo consists of a blue circle with a white "A" inside of it, followed by the word "Auxein" in blue, with a registered trademark symbol next to it. The logo is simple and clean, and the blue color gives it a professional look.
3.5mm Wise-Lock Extra-Articular Distal Humerus Plate
3.5mm Wise-Lock Extra-Articular Distal Humerus Plate are indicated for fractures of the distal humerus.
PHEELOS-3.5mm Wise-Lock Proximal Humerus Plate, Short & Long
PHEELOS Short Indications
- Dislocated two-, three-, and four-fragment fractures of the proximal humerus
- Pseudarthroses in the proximal humerus
- Osteotomies in the proximal humerus
PHEELOS long indications
• As for PHEELOS Short, but for fractures extending to the shaft or without medial support.
3.5mm Wise-Lock Proximal Humerus Plate
The 3.5mm Wise-Lock Proximal Humerus Plate is intended for fractures and fracture dislocations, osteotomies, and nonunions of the proximal humerus.
3.5mm Wise-Lock Periarticular Proximal Humerus Plate
3.5mm Wise-Lock Periarticular Proximal Humerus Plate are indicated for fractures, fracture dislocations, osteotomies, and nonunions of the proximal humerus.
3.5mm Wise-Lock Olecranon Plate
3.5mm Wise-Lock Olecranon Plate is indicated for fixation of fractures, osteotomies and non-unions of the olecranon.
3.5mm Wise-Lock Hook Plate
3.5mm Wise-Lock Hook Plate is indicated for fractures, osteotomies and non-unions of small bones including the ulna, radius, tibia and fibula.
A.6) Summary of Technological Characteristics as compared to the predicate devices: Substantial equivalence including comparison with predicate devices.
A comparison between the Auxein's Humerus and Ulna System and predicate devices has been performed which has resulted in demonstration of similarities in dimensional and performance criteria.
| S.No. | Characteristics | Auxein Device | Predicate Device | Remarks |
|---|---|---|---|---|
| 1. | Product | |||
| Code | HWC (Primary), HRS | HWC (Primary), HRS | Identical | |
| as | ||||
| predicate | ||||
| device | ||||
| 2. | Regulation | |||
| Number | 21 CFR 888.3030 (Primary), | |||
| 21 CFR 888.3040 | 21 CFR 888.3030 (Primary), 21 | |||
| CFR 888.3040 | Identical | |||
| as | ||||
| predicate | ||||
| device | ||||
| 3. | Regulatory | |||
| Class | Class II | Class II | Identical | |
| as | ||||
| predicate | ||||
| device | ||||
| 4. | Indications | |||
| for use | 2.7/3.5mm Wise-Lock | |||
| Dorsolateral Distal | ||||
| Humerus Plate | ||||
| 2.7/3.5mm Wise-Lock | ||||
| Dorsolateral Distal Humerus | ||||
| Plate is intended for treating | ||||
| fractures of humerus bones. | 2.7/3.5mm Wise-Lock | |||
| Dorsolateral Distal Humerus | ||||
| Plate | ||||
| 2.7/3.5mm Wise-Lock Dorsolateral | ||||
| Distal Humerus Plate is intended | ||||
| for treating fractures of humerus | ||||
| bones. | Identical | |||
| as | ||||
| predicate | ||||
| device. | ||||
| 2.7/3.5mm Wise-Lock | ||||
| Dorsolateral Distal | ||||
| Humerus Plate with Lateral | ||||
| Support | ||||
| 2.7/3.5mm Wise-Lock | ||||
| Dorsolateral Distal Humerus | ||||
| Plate with Lateral Support is | ||||
| intended for treating fractures | ||||
| of humerus bones. | 2.7/3.5mm Wise-Lock | |||
| Dorsolateral Distal Humerus | ||||
| Plate with Lateral Support | ||||
| 2.7/3.5mm Wise-Lock Dorsolateral | ||||
| Distal Humerus Plate with Lateral | ||||
| Support is intended for treating | ||||
| fractures of humerus bones. | ||||
| 2.7/3.5mm Wise-Lock | ||||
| Dorsolateral Medial Distal | ||||
| Humerus Plate | ||||
| 2.7/3.5mm Wise-Lock | ||||
| Dorsolateral Medial Distal | ||||
| Humerus Plate are indicated | ||||
| for intra articular fractures of | ||||
| the distal humerus, | ||||
| commninuted supracondylar | ||||
| fractures, osteotomies, and | ||||
| non-unions of the distal | ||||
| humerus. | 3.5 mm LCP Distal Humerus | |||
| System | ||||
| 3.5 mm LCP Distal Humerus | ||||
| System are indicated for intra | ||||
| articular fractures of the distal | ||||
| humerus, commninuted | ||||
| supracondylar fractures, | ||||
| osteotomies, and non-unions of the | ||||
| distal humerus. | ||||
| 3.5mm Wise-Lock Extra- | ||||
| Articular Distal Humerus | ||||
| Plate | ||||
| 3.5mm Wise-Lock Extra- | ||||
| Articular Distal Humerus | ||||
| Plate are indicated for intra | ||||
| articular fractures of the distal | 3.5mm LCP Extra-Articular | |||
| Distal Humerus Plate | ||||
| 3.5mm LCP Extra-Articular Distal | ||||
| Humerus Plate are indicated for | ||||
| intra articular fractures of the distal | ||||
| humerus, commninuted | ||||
| supracondylar fractures, | ||||
| osteotomies, and non-unions of the | ||||
| distal humerus. | ||||
| PHEELOS-3.5mm Wise-Lock | ||||
| Proximal Humerus Plate, Short |
Following is the summary of parameters in which the comparison has been verified:
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Image /page/9/Picture/1 description: The image shows the logo for Auxein. The logo consists of a blue circle with a white "A" inside of it. To the right of the circle is the word "Auxein" in blue, with a small "R" in a circle above the "n".
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Image /page/10/Picture/1 description: The image contains the logo for Auxein. The logo consists of a stylized letter "A" inside of a circle, followed by the word "Auxein" in a sans-serif font. A registered trademark symbol is located to the right of the word "Auxein". The logo is blue.
| humerus, commninuted
supracondylar fractures,
osteotomies, and non-unions
of the distal humerus. | & Long
PHEELOS-3.5mm Wise-Lock
Proximal Humerus Plate, Short &
Long are intended for treating
fractures of humerus bones. |
|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| PHEELOS-3.5mm Wise-
Lock Proximal Humerus
Plate, Short & Long | 3.5mm Wise-Lock Proximal
Humerus Plate |
| PHEELOS-3.5mm Wise-
Lock Proximal Humerus
Plate, Short & Long are
intended for treating fractures
of humerus bones. | The 3.5mm Wise-Lock Proximal
Humerus Plate is intended for
treating fractures of humerus
bones. |
| 3.5mm Wise-Lock Proximal
Humerus Plate | 3.5mm LCP Periarticular
Proximal Humerus Plates |
| The 3.5mm Wise-Lock
Proximal Humerus Plate is
intended for treating fractures
of humerus bones. | 3.5mm LCP Periarticular Proximal
Humerus Plate are indicated for
fractures, fracture dislocations,
osteotomies, and nonunions of the
proximal humerus, particularly in
osteopenic bone. |
| 3.5mm Wise-Lock
Periarticular Proximal
Humerus Plate | 3.5mm LCP Olecranon Plate |
| 3.5mm Wise-Lock
Periarticular Proximal
Humerus Plate are indicated
for fractures, fracture
dislocations, osteotomies, and
nonunions of the proximal
humerus. | The Synthes 3.5 mm Locking
Compression Plate (LCP) System
is indicated for fixation of
fractures, osteotomies and non-
unions of the clavicle, scapula,
olecranon, humerus, radius, ulna,
pelvis, distal tibia, fibula,
particularly in osteopenic bone for
adult patients. |
| 3.5mm Wise-Lock
Olecranon Plate | 3.5 mm LCP Hook Plate |
| 3.5mm Wise-Lock Olecranon
Plate is indicated for fixation
of fractures, osteotomies and
non-unions of the olecranon. | 3.5mm LCP Hook Plate is
indicated for fractures, osteotomies
and non-unions of small bones
including the ulna, radius, tibia and
fibula, particularly in osteopenic
bone. |
| 3.5mm Wise-Lock Hook
Plate | |
| 3.5mm Wise-Lock Hook
Plate is indicated for
fractures, osteotomies and | |
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Image /page/11/Picture/1 description: The image shows the logo for Auxein. The logo consists of a stylized letter "A" inside a circle, followed by the word "Auxein" in a stylized font. The entire logo is in blue.
| | | non-unions of small bones
including the ulna, radius,
tibia and fibula. | | |
|-----|-----------------------------|---------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------|------------------------------------------------|
| 5. | Material | Titanium Alloy and Stainless Steel. | Titanium Alloy and Stainless Steel. | Confirm to
the same
material
standard |
| 6. | Performance
Standards | The performance testing was
done on the subject device as
per the standard ASTM F382
and F543. | The performance testing was done
on the predicate device as per the
standard ASTM F382 and F543. | Identical
as
predicate
device. |
| 7. | Sterilization | Gamma Sterilization Method
and Non-Sterile used in
subject device. | Gamma Sterilization Method and
Non-Sterile used in predicate
device. | Identical
as
predicate
device. |
| 8. | Shelf-life | 5 Years (For Sterilized
Product) | 5 Years (For Sterilized Product) | Identical
as
predicate
device. |
| 9. | Single
Use/Reuse | Single Use | Single Use | Identical
as
predicate
device. |
| 10. | Operating
Principle | The plate is fixed to the bone
by application of screws on
both sides of the fracture. | The plate is fixed to the bone by
application of screws on both sides
of the fracture. | Identical
as
predicate
device. |
| 11. | Dimensional
Verification | The same dimensions are found in both new devices as well as
Predicate devices. | | Identical
as
predicate
device. |
B.1) Discussion on the non-clinical testing performed
Following are the applicable product standards considered for non-clinical standards:
- Material Standards. .
- Biocompatibility Standards
- . Performance Standards.
- Sterilization, shelf-life and packaging for sterile product.
- Bacterial Endotoxin
Non-Clinical Test Summary:
Bench tests were conducted to verify that the subject device met all design specifications. The test results demonstrated that the subject device complies with the following standards:
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Image /page/12/Picture/1 description: The image shows the logo for Auxein. The logo consists of a blue circle with a stylized "A" inside of it, followed by the word "Auxein" in blue, stylized font. There is a small "R" in a circle to the right of the word "Auxein".
Material Standards:
The material standards are the essential part to be complied with first, as it is the basis of manufacturing metallic surgical implants.
We have complied with the following material standards:
- . ASTM F136/ISO 5832-3: Standard specification for wrought Titanium-6 Aluminum-4 Vanadium ELI (Extra low interstitial) Alloy for surgical implant applications.
- ASTM F899-12: Standard Specification for Wrought Stainless Steels for surgical instruments. ●
- ASTM F138/ISO 5832-1: Standard Specification for Wrought-18 Chromium-14 Nickel-2.5 . Molybdenum Stainless Steel Bar and Wire for Surgical Implants.
Note: We have used Grade 304 of Stainless steel (SS 304) Material for instruments as per ASTM F899-12b, Stainless Steel (Grade 316L) as per ISO 5832-3/ASTM F138 for Stainless Steel Implants and Titanium Alloy (Ti-6Al-4V) Grade 5 as per ISO 5832-1/ASTM F136 for Titanium Implants.
We have verified the purchased material and are in compliance to these standards and copies of the relevant test results are attached in Vol_005_Appendix D Implant Material Report and Vol_006_ Appendix E ASTM F899 Report of the technical dossier.
Summary of Biocompatibility
The device in its final finished form has been evaluated for biocompatibility according to ISO 10993.
Mechanical performance
- ASTM F382, Standard Specification and Test Method for Metallic Bone Plates. .
- ASTM F543, Standard Specification and Test Method for Metallic Medical Bone Screws. .
The following tests were performed with the predicate device:
Plate
- •
Screw
- . Driving Torque Test: Conforms
- Torsion Test: Conforms ●
- Axial Pull-out Test: Conforms
The results of this testing indicate that the Humerus and Ulna System is equivalent to the predicate device.
Sterilization, shelf-life and packaging for sterile product
- ISO 11137-1:2006, sterilization of health care products Radiation Part 1: Requirements for . development, validation and routine control of a sterilization process for medical devices.
- · ISO 11137-2:2012, Sterilization of health care products Radiation Part 2: Establishing the sterilization dose.
- ISO 11137-3:2017, Sterilization of health care products Radiation Part 3: Guidance on ●
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K213108
Image /page/13/Picture/1 description: The image shows the logo for Auxein. The logo consists of a blue circle with a stylized "A" inside of it. To the right of the circle is the word "Auxein" in blue, with a small "®" symbol in the upper right corner of the word. The logo is simple and modern, and the blue color gives it a sense of trust and reliability.
dosimetric aspects of development, validation and routine control.
- . ISO 17665-1:2006, Sterilization of health care products - Moist heat -- Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices.
- ISO/TS 17665-2:2009, Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1.
- ISO/TS 17665-3:2013(en), Sterilization of health care products - Moist heat - Part 3: Guidance on the designation of a medical device to a product family and processing category for steam sterilization.
- . ISO 11140-1:2014, Sterilization of health care products — Chemical indicators — Part 1: General requirements.
- . ISO 11737-1:2018 Sterilization of medical devices - Microbiological methods- Part 1: Estimation of population of microorganisms on products.
- ISO 11737-2:2009 Sterilization of medical devices - Microbiological methods- Part 2: Tests of sterility performed in the validation of a sterilization process.
- ISO 11607-1:2006/AMD1:2014 Packaging for terminally sterilized medical devices - part 1:requirements for materials, sterile barrier systems and packaging system.
- ISO 11607-2:2006/AMD1:2014 Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes.
- ASTM F1980:2016 Standard Guide for Accelerated Aging of Sterile Barrier Systems for Medical ● Devices.
- ASTM F88/F88M:2015 Standard test method for seal strength of flexible barrier materials.
- ASTM F1929:2015 Standard Test Method for Detecting Seal Leaks in Porous Medical Packaging by Dye Penetration.
Bacterial Endotoxin
- USP Bacterial Endotoxin Test. ●
- USP Medical Devices-Bacterial Endotoxin and Pyrogen Tests.
Conclusion:
There are no significant differences between the subject device and the predicate devices that would adversely affect the use of the product. It is substantially equivalent to these devices in design, function, materials, and operational principles as internal fixation components. From the data available we can justify that the Auxein's Humerus and Ulna is as safe, and as effective and perform the same indications for use as those of already marketed predicate devices identified in A.3. of 510(k) summary.