(121 days)
No
The device description focuses on mechanical components (plates, screws, instruments) and bench testing for structural integrity. There is no mention of software, algorithms, or data processing that would indicate AI/ML.
No.
The ARIX Foot System is a rigid internal fixation device (plates and screws) used for orthopedic procedures such as reconstruction, arthrodesis, and fracture treatment, rather than providing direct therapy or treatment itself.
No
The ARIX Foot System is described as rigid fixation consisting of plates and screws intended for internal fixation, reconstruction, or arthrodesis. It is a surgical implant and instrumentation system, not a device designed to diagnose conditions.
No
The device description explicitly states it is a system of rigid fixation consisting of plates, screws, and various manual surgical instruments made of titanium, which are physical hardware components.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In Vitro Diagnostics are medical devices used to perform tests on samples taken from the human body (like blood, urine, or tissue) to provide information about a person's health.
- ARIX Foot System Function: The ARIX Foot System is a system of plates and screws intended for internal fixation, reconstruction, or arthrodesis of bones in the foot and ankle. It is a surgical implant used directly within the body to provide structural support and stability.
- Lack of Diagnostic Testing: The description of the ARIX Foot System does not mention any function related to testing samples or providing diagnostic information. Its purpose is purely mechanical and structural within the body.
Therefore, based on the provided information, the ARIX Foot System is a surgical implant, not an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
The ARIX Foot System is intended for use in internal fixation, reconstruction, or arthrodesis of small bones including the fore, mid- and hind foot and ankle. Examples of these procedures may include but are not limited to replantation, lag screw techniques, joint fusions, corrective osteotomies, and the treatment of fractures.
Product codes
HRS
Device Description
The ARIX Foot System is rigid fixation consisting of plates and screws in various configurations, shapes and sizes. The ARIX Foot System is made of Unalloyed Titanium and Titanium Alloy (Ti-6AL-4V), which meet ASTM F67, Standard Specification for Unalloyed Titanium for Surgical Implant Applications, and ASTM F136, Standard Specification for Wrought Titanium-6 Aluminum-4 Vanadium ELI (Extra Low Interstitial) Alloy for Surgical Implant Applications. The plates vary essentially through different lengths and number of plate holes. The screws are self-tapping with various diameters, which are applied with the reconstruction locking screws together. The Cortical Screws & locking screws are provided with diameter 2.8 mm to 3.5 mm and lengths from 8 mm to 50 mm, lag screws (Cannulated and Cannulated Headless Types) with diameters of 1.5 mm to 6.0 mm and lengths of 8 mm to 80 mm. It also includes various manual surgical instruments, such as guide pins, drill guides, drill bits and driver shafts, washers, drill sleeve, depth gauge, bender, cleaning stylet and handbody. The ARIX Foot System is not provided sterile. It is required to be sterilized via autoclave method to reach a SAL of 10 by the hospital prior to surgery. The sterilization method is presented in the instruction, which was validated per 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. This device performance is not adversely affected by aging or storage conditions since this device is to be sterilized at the hospital before use and also to be single use.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
small bones including the fore, mid- and hind foot and ankle
Indicated Patient Age Range
Not Found
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)
Non-Clinical Test Summary: Bench tests were conducted to verify that the proposed device met all design specifications. The test results demonstrated that the proposed device complies with the following standards: ASTM F 382-99. Standard Specification and Test Method for Metallic Bone Plates; ASTM F 543-07. Standard Specification and Test Methods for Metallic Medical Bone Screws. The following tests were performed with the predicate device: Plates (Tensile strength test, Bending strength test per ASTM F382) and Screws (Driving torque test per ASTM F543, Axial pull-out test per ASTMV F543, Torsion test per ASTM F543). The results of this testing indicate that the ARIX Foot System is equivalent to predicate device.
Clinical Test Summary: No clinical studies were considered necessary and performed.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
K063875, K023360, K023365, K112457
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
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
#702, Kolon Science Guro-Dong, Guro-Gu, Seoul, 152-05 Tel : +82 2 850 3500 / Fax : +82 2 850 3535
510(k) Summary
[As required by 21 CFR 807.92]
1. Date Prepared [21 CFR 807.92(a)(1)]
Address:
K131311 page 1 of 4
2 May 2013
2. Submitter's Information [21 CFR807.92(a)(1)]
- Jeil Medical Corporation . Name of Sponsor:
SEP 0 5 2013
#702, Kolon Science Valley 2nd 811, Guro-dong, Guro-gu Seoul, 152-050, Korea
.
- Ji-Eun Kim (Ms.) / RA Manager Contact Name: .
- Telephone No. : +82 2 850 3500 l
- Fax No. : +82 2 850 3525 -
- jekim@jeilmed.co.kr Email Address : -
- Registration Number: 3004049923 .
- Same as Sponsor . Name of Manufacturer:
- Address: Same as Sponsor .
3. Trade Name, Common Name, Classification [21 CFR 807.92(a)(2)]
ll
- Common Name: Bone plates and screws .
- Classification Name: Single/multiple component metallic bone fixation . appliances and accessories
ARIX Foot System
- Classification Panel: Orthopedic .
- Classification Requlation: 21 CFR 888.3030 .
- Product Code: HRS .
- Device Class: .
Device Description
.
Trade Name:
1
#702, Kolon Science Valley 2 811 Guro-Dong, Guro-Gu, Seoul, 152-050 Korea Tel : +82 2 850 3500 / Fax : +82 2 850 3535
K131311 page 2 of 4
4. Identification of Predicate Device(s) [21 CFR 807.92(a)(3)[
The identified predicate devices within this submission is shown as follows:
| • 510(k) Number: | K063875 |
|---|---|
| • Applicant: | Howmedica Osteonics Corp. |
| • Common Name: | Bone plates and screws |
| • Device Name: | Stryker Foot Plating System |
| • 510(k) Number: | K023360 |
| • Applicant: | Jeil Medical Corporation |
| • Common Name: | Bone fixation plates |
| • Device Name: | Leforte System Bone Plate |
| • 510(k) Number: | K023365 |
| • Applicant: | Jeil Medical Corporation |
| • Common Name: | Bone fixation screws |
| • Device Name: | Leforte System Bone Screw |
| • 510(k) Number: | K112457 |
- 510(k) Number: .
- Applicant: .
- . Common Name:
- . Device Name:
- K11245/
Jeil Medical Corporation Bone fixation Plates & Screws Leforte System Bone Plate & Screw
There are no significant differences between the Model ARIX Foot System and the predicate device 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.
5. Description of the Device [21 CFR 807.92(a)(4)]
The ARIX Foot System is rigid fixation consisting of plates and screws in various configurations, shapes and sizes, as follows:
| | Plate | Cortical
Screw | Locking Screw | Lag Screw
(Cannulated
Type) | Lag Screw
(Cannulated
Headless
Type) |
|------------------------|------------------------------------|--------------------------------------------------|----------------------------------------------|----------------------------------------------|------------------------------------------------|
| Type/
Configuration | F28-Series | 28-FC-Series | 28L-HF-Series | 23-CS-Series,
30-CS-Series | 15-CH-Series,
23-CH-Series,
30-CH-Series |
| | F35-Series | 35-FC-Series | 35L-HF-Series | 45-CS-Series,
60-CS-Series | 30-CH-Series |
| Material | ASTM F67,
Unalloyed
Titanium | ASTM F 136,
Titanium
Alloy (Ti-6Al-
4V) | ASTM F 136,
Titanium Alloy
(Ti-6Al-4V) | ASTM F 136,
Titanium Alloy
(Ti-6Al-4V) | ASTM F 136,
Titanium Alloy
(Ti-6Al-4V) |
Device Description
2
- Kolon Science Valle Guro-Dong, Guro-Gu, Seoul, 152-050 Tel : +82 2 850 3500 / Fax : +82 2 850 3535
The ARIX Foot System is made of Unalloyed Titanium and Titanium Alloy (Ti-6AL-4V), which meet ASTM F67, Standard Specification for Unalloyed Titanium for Surgical Implant Applications, and ASTM F136, Standard Specification for Wrought Titanium-6 Aluminum-4 Vanadium ELI (Extra Low Interstitial) Alloy for Surgical Implant Applications, which are widely used for surgical implants with well-known biocompatibility.
The plates vary essentially through different lengths and number of plate holes. The screws are self-tapping with various diameters, which are applied with the reconstruction locking screws together. The Cortical Screws & locking screws are provided with diameter 2.8 mm to 3.5 mm and lengths from 8 mm to 50 mm, lag screws (Cannulated and Cannulated Headless Types) with diameters of 1.5 mm to 6.0 mm and lengths of 8 mm to 80 mm.
It also includes various manual surgical instruments, such as guide pins, drill guides, drill bits and driver shafts, washers, drill sleeve, depth gauge, bender, cleaning stylet and handbody.
The ARIX Foot System not provided sterile. It is required to be sterilized via autoclave method to reach a SAL of 10 by the hospital prior to surgery. The sterilization method is presented in the instruction, which was validated per 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.
This device performance is not adversely affected by aging or storage conditions since this device is to be sterilized at the hospital before use and also to be single use.
6. Intended Use [21 CFR 807.92(a)(5)]
The ARIX Foot System is intended for use in internal fixation, reconstruction, or arthrodesis of small bones including the fore, mid- and hind foot and ankle. Examples of these procedures may include but are not limited to replantation, lag screw techniques, joint fusions, corrective osteotomies, and the treatment of fractures.
7. Technological Characteristics [21 CFR 807.92(a){6)]
ARIX Foot System, Bone Plates: Based on a technical feature comparison, the subject device was found to be similar to all predicate devices with regard to design and materials. The subject plates also have a polyaxial locking feature, similar to the design used in the predicate device (K063875).
ARIX Foot System, Bone Screws: They share similar head, neck, and thread designs as the smaller screws that are currently cleared under the predicate device (K063875).
Non-Clinical Test Summary:
Bench tests were conducted to verify that the proposed device met all design specifications. The test results demonstrated that the proposed device complies with the following standards:
Device Description
Page 21 of 94
3
K131311 page 4 of 4
- Kolon Science Valley Guro-Dong, Guro-Gu, Seoul, 152-050 Korea Tel : +82 2 850 3500 / Fax : +82 2 850 3535
- ASTM F 382-99. Standard Specification and Test Method for Metallic Bone Plates �
- ASTM F 543-07. Standard Specification and Test Methods for Metallic Medical Bone . Screws
The following tests were performed with the predicate device:
- . Plates
- Tensile strength test ।
- Bending strength test per ASTM F382
- Screws .
- Driving torque test per ASTM F543 ।
- Axial pull-out test per ASTMV F543 ।
- Torsion test per ASTM F543 ।
The results of this testing indicate that the ARIX Foot System is equivalent to predicate device.
Clinical Test Summary
No clinical studies were considered necessary and performed.
8. Substantial Equivalence [21 CFR 807.92(b)(1) and 807.92]
When compared to the predicate device (K063875), the ARIX Foot System presented in this submission has the same:
- . Intended Use
- Technological characteristics .
- Operating principle .
- . Design features
- Performance ●
- Biocompatibility .
- Materials .
- Method of sterilization and sterility assurance level .
9. Conclusion [21 CFR 807.92(b)(3)]
In all respects, the ARIX Foot System is the equivalent of currently marketed devices. This device is made of the same materials and have similar dimensions and characteristics. This device is manufactured from material of the unalloyed titanium and titanium alloy that is used generally in this kind of bone plate/screw system. This device, ARIX Foot System, is substantially equivalent in design, material, and function to the predicate device.
Device Description
4
DEPARTMENT OF HEALTH & HUMAN SERVICES
Public Health Service
September 5, 2013
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20093-0002
Jeil Medical Corporation Ms. Ji-Eun Kim RA Manager Number 702 Kolon Science Valley 2nd 811 Guro-Dong, Guro-Gu Scoul. Republic of Korea, Korea 152-050
Re: K131311 Trade/Device Name: ARIX Foot 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 Dated: July 30, 2013 Received: August 1. 2013
Dear Ms. Kim:
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 10 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. The general controls provisions of the Act include requirements for annual registration. Iisting of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH docs 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 cither 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.
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
5
Page 2 - Ms. Ji-Eun Kim
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 (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820): and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Small Manufacturers. International and Consumer Assistance at its toll-. free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part
807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803). please go to
http://www.fda.gov/MedicalDevices/Safety/ReportalProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDeviccs/ResourcesforYou/Industry/dcfault.htm.
Sincerely vours.
Mark N. Melkerson -S
Mark N. Melkerson Director Division of Orthopedic Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
6
Indications for Use
510(k) Number (if known): K131311
Device Name: ARIX Foot System
Indications for Use:
The ARIX Foot System is intended for use in internal fixation, reconstruction, or arthrodesis of small bones including the fore, mid- and hind foot and ankle. Examples of these procedures may include but are not limited to replantation, lag screw techniques, joint fusions, corrective osteotomies, and the treatment of fractures.
.
Prescription Use × (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Page 1 of 1
Elizabeth L. Frank -S