(167 days)
No
The device description focuses on mechanical components for fracture fixation and stabilization, with no mention of AI or ML capabilities. The predicate devices are also traditional mechanical systems.
Yes
This device is a medical implant designed to stabilize bone fractures, specifically in the proximal femur, and aid in the healing process until bony union occurs. This aligns with the definition of a therapeutic device as it is used to treat or manage a medical condition.
No
This device is a surgical implant designed to fix and stabilize bone fractures, not to diagnose medical conditions.
No
The device description clearly outlines a system of physical components (lag screws, compression screws, side plates, etc.) made of materials like Titanium Alloy and Stainless Steel, intended for surgical implantation. There is no mention of software as a component or the primary function of the device.
Based on the provided text, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states the device is for the "fixation/stabilization of intertrochanteric fractures, some high subtrochanteric fractures and intracapsular fractures" and to "stabilize fragments of the fracture until bony union can occur." This describes a surgical implant used directly on the patient's body to treat a physical condition.
- Device Description: The description details a "cannulated lag and compression screw system to be used with a side plate for fracture fixation and stabilization of the proximal femur." It describes physical components like screws, plates, and instruments used in surgery.
- Lack of IVD Characteristics: There is no mention of the device being used to examine specimens derived from the human body (like blood, urine, tissue, etc.) to provide information for diagnosis, monitoring, or screening.
IVD devices are used in vitro (outside the body) to analyze biological samples. This device is used in vivo (inside the body) as a surgical implant.
N/A
Intended Use / Indications for Use
The ODi Compression Hip Screw System will be used on indications that are common with presently marketed compression hip screw systems. The primary indications are for fixation/stabilization of intertrochanteric fractures, some high subtrochanteric fractures, and intracapsular fractures, provided that weight bearing is not allowed until the fracture shows evidence of union. The device is intended to stabilize fragments of the fracture until bony union can occur.
Product codes
KTT
Device Description
The Orthopedic Designs, Inc. Compression Hip Screw System is a cannulated lag and compression screw system to be used with a side plate for fracture fixation and stabilization of the proximal femur until bony union can occur. The system includes a lag screw that may be utilized alone with a side plate, or for compression of a fracture, may be used with a compression screw.
Each system shall consist of the same material when used and shall not be mixed. Titanium Alloy and Stainless Steel within the same use.
The distal end of the lag screws are keyed, but not threaded, thereby allowing the screw to slide within the barrel of the side plate while preventing rotation of the lag screw within the head of the femur. Immediate compression may be obtained with the use of a compression screw threaded into the inner canal of the lag screw.
A compression screw locking mechanism called a jam screw is also available, providing a safe mechanism to lock the compression screw in place. The jam screw will prevent a common natural migration of the compression screw from the lag attachment.
The side plates, lag screws, compression screws, cortical bones screws and instruments are similar in design, materials and intended use to other 510(k) cleared devices/instruments which are in commercial distribution.
A range of system component sizes and lengths will be made available, offering a range of fracture compression. The components are designed to be manually or mechanically inserted using common (e.g. American Orthopedic) manual and power instrumentation.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
proximal femur
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)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
K781762, K823548, K900584, K850886, K872223, K955306, K922295, K791619, K861178, K946156
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
Premarket Notification
510(k) Summary of Safety and Effectiveness Information
NOV | 2 |997
For Release Upon Request Only
| Date of Preparation: | September 17, 1997 |
|---|---|
| Regulatory Authority: | Safe Medical Devices Act of 1990, 21 CFR 807.92 |
| Company Name / Contact: | |
| Company: | ODi (Orthopedic Designs, Inc.) |
| 5501-D Airport Boulevard | |
| Tampa, FL 33634 | |
| Contact: | Randy Lawson, Vice President, COO |
| (813) 889-9194 | |
| Establishment Registration Number: | The registration number for |
| Orthopedic Designs, Inc. is | |
| pending | |
| Classification Name: | Appliance, Fixation, Nail/Blade/Plate |
| Combination, Multiple Component | |
| Classification Reference: | 21 CFR § 888.3030 |
| Common Used Name: | Orthopaedic Compression Bone Screw |
| Device Product Code: | KTT |
| Classification Panel: | 87 - Orthopaedic and Rehabilitation Devices |
| Trade Proprietary Name: | ODi Compression Hip Screw System |
Proposed Regulatory Class:
The FDA has classified similar products as a Class II device by the Orthopedic Device Section of the Surgical and Rehabilitation Devices Panel at Section 888-3030. The product code generally referred to is KTT ( Product Code: KTT ), and ODi submits this application under this designation.
1
Performance Standards:
No performance standards applicable to the fixation bone screw have been established by the FDA. However, the titanium alloy 6AL-4V ELI alloy or the 316-L stainless steel used to manufacture the ODi Compression Hip Screw System meets the chemical and mechanical requirements in voluntary standards established by the American Society for Testing and Materials (ASTM F136-92 and ASTM F138-92), respectively.
Package and Labeling:
Package labeling has been developed to industry standards. Packaging is also standard commercially available type quality and is stored in a fashion which prevents damage to the container or package.
Device Description:
The Orthopedic Designs, Inc. Compression Hip Screw System is a cannulated lag and compression screw system to be used with a side plate for fracture fixation and stabilization of the proximal femur until bony union can occur. The system includes a lag screw that may be utilized alone with a side plate, or for compression of a fracture, may be used with a compression screw.
Each system shall consist of the same material when used and shall not be mixed. Titanium Alloy and Stainless Steel within the same use.
The distal end of the lag screws are keyed, but not threaded, thereby allowing the screw to slide within the barrel of the side plate while preventing rotation of the lag screw within the head of the femur. Immediate compression may be obtained with the use of a compression screw threaded into the inner canal of the lag screw.
A compression screw locking mechanism called a jam screw is also available, providing a safe mechanism to lock the compression screw in place. The jam screw will prevent a common natural migration of the compression screw from the lag attachment.
The side plates, lag screws, compression screws, cortical bones screws and instruments are similar in design, materials and intended use to other 510(k) cleared devices/instruments which are in commercial distribution.
A range of system component sizes and lengths will be made available, offering a range of fracture compression. The components are designed to be manually or mechanically inserted using common (e.g. American Orthopedic) manual and power instrumentation.
2
Indications for Use:
The ODi Compression Hip Screw will be used on indications that are common with presently marketed compression hip screw systems. The primary indications are for fixation/stabilization of intertrochanteric fractures, some high subtrochanteric fractures, and intracapsular fractures, provided that weight bearing is not allowed until the fracture shows evidence of union. The device is intended to stabilize fragments of the fracture until bony union can occur.
Contra-indications for Use:
The ODi Compression Hip Screw System is not intended for use in patients with the following conditions:
-
- Active local Infection.
-
- Metal sensitivity or allergic reaction to foreign bodies.
-
- Other conditions that may place the patient at risk.
-
- When quality of bone stock prevents secure seating of the screws.
Substantial Equivalent Devices:
Orthopedic Designs, Inc. believes the ODi Compression Hip Screw System is substantially equivalent to the products described herein with respect to indications for use, device design, materials, method of manufacture and method of sterilization. Within the proposed class, the following devices are used as predicate devices for comparison:
| Howmedica Compression Hip Screw System | (K781762) |
|---|---|
| Howmedica Compression Hip Screw Sideplate | (K823548) |
| Howmedica Alta Lag Screw & Compression Screw | (K900584) |
| Howmedica Omega Compression Screw System | (K850886), |
| (K872223) | |
| Howmedica Omega+ Compression Hip Screw System | (K955306) |
| Howmedica Omega Plus Compression Hip System | (K922295) |
| Synthes DHS Hip Screw | (K791619) |
| Ace Cannulated Hip Screw and Captured Hip Screw System | |
| Richards KeyLock System | |
| Richards Kwik-Key | |
| Richards Ambi Compression Hip Screw | |
| Richards Classic | |
| Zimmer Compression Hip Screw with ECT | |
| Zimmer Free-Lock | |
| Zimmer Versa-Fx | |
| Orthopedic Equipment Company's (OFCO C.) Compression Hip Screw Plate |
3
Wright Hip Compression Screw/Plate Wright Concise Compression Hip Screw System Wright Cannulated Plus Screw System Depuy Combined NoLok /Keyed Compression Hip Screw System (K861178), (K946156)
Each of these products are commercially available and marketed Class II devices indicated for use for intertrochanteric fractures, some high subtrochanteric fractures, and intracapsular fractures. The ODi Compression Hip Screw System is also labeled for similar use.
4
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
NOV 1 2 1997
Mr. Randy Lawson ·Vice President, COO Orthopedic Designs, Inc. 5501-D Airport Boulevard Tampa, Florida 33634-5303
Re : K971993 Trade Name: ODi Compression Hip Screw System Requlatory Class: II Product Code: KTT Dated: September 18, 1997 Received: September 22, 1997
Dear Mr. Lawson:
We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to 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). You may, therefore, market the device, subject to the general controls provisions of the Act. The qeneral controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major requlations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. ਚੇ substantially equivalent determination assumes compliance with the current Good Manufacturing Practice requirement, as set forth in the Quality System Requlation (QS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic (QS) inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.
5
Page 2 - Mr. Randy Lawson
This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4659. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html".
Sincerely yours,
C. Colin M. Wittner, Ph.D.
Celia M. Witten, Ph.D., M.D. Director Division of General and Restorative Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
6
K971993 510(k) Number:
Device Name: ODi Compression Hip Screw System
Indications For Use:
The ODi Compression Hip Screw System will be used on indications that are common with presently marketed compression hip screw systems. The primary indications are for fixation/stabilization of intertrochanteric fractures, some high subtrochanteric fractures and intracapsular fractures, provided that weight bearing is not allowed until the fracture shows evidence of union. The device is intended to stabilize fragments of the fracture until bony union can occur.
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
| (Division Sign-Off) | |
|---|---|
| Division of General Restorative Devices | |
| 510(k) Number | K971893 |
| Prescription Use (per 21 CFR 801.109) | X |
|---|---|
| --------------------------------------- | --- |
OR
Over-The-Counter Use
(Optional Format 1-2-96)