← Product Code [JDI](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/JDI) · K965019

# THE C-FIT FEMORAL HIP SYSTEM (K965019)

_Corin USA · JDI · Mar 25, 1997 · Orthopedic · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/JDI/K965019

## Device Facts

- **Applicant:** Corin USA
- **Product Code:** [JDI](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/JDI.md)
- **Decision Date:** Mar 25, 1997
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 888.3350
- **Device Class:** Class 2
- **Review Panel:** Orthopedic
- **Attributes:** Therapeutic

## Intended Use

The devices are used to resurface the femoral hip joint and reconstitute function following the degenerative effects of osteo and rheumatoid arthritis, post trauma disease effects, avascular necrosis and septic or aseptic total hip revision. The C-Fit plasma sprayed femoral components are intended for use with bone cement only.

## Device Story

Femoral hip system; includes standard and long stem options; optional calcar collars; plasma-sprayed cobalt chrome coating for mechanical interlock with PMMA bone cement. Manufactured from cobalt chrome alloy. Used in orthopedic surgery to resurface femoral hip joint; reconstitutes function post-degeneration. Compatible with Corin cobalt chrome modular heads, bipolar, or uni-polar devices. Intended for cemented use only. Surgeon-operated in clinical/OR setting; provides structural support for hip joint; improves patient mobility/function.

## Clinical Evidence

No clinical trials presented. Device has approximately 10 years of clinical use outside the U.S. with no reported significant post-operative problems. Safety supported by extensive mechanical bench testing.

## Technological Characteristics

Materials: Cobalt chrome alloy stem with cobalt chrome plasma spray coating. Design: Standard and long stem options, with/without calcar collars. Intended for use with PMMA bone cement. Mechanical interlock via increased surface roughness from plasma spray.

## Regulatory Identification

A hip joint metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a hip joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and an acetabular resurfacing component made of ultra-high molecular weight polyethylene and is limited to those prostheses intended for use with bone cement (§ 888.3027).

## Predicate Devices

- V.S.P. (C-Fit stem) Hip system (Corin Medical Ltd.)

## Reference Devices

- Mallory/head system (Biomet)

## Submission Summary (Full Text)

> This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com.
>
> Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/).

{0}

Page 8
K965019

# 510(k) SUMMARY

MAR 25 1997

**Name of Company:** Corin Medical Ltd.
The Corinium Centre
Cirencester
Gloucestershire GL7 1YJ
United Kingdom

**Name of Device:** The C-Fit Femoral Hip System

**Device Description:** A femoral hip system consisting of standard and long stem options with or without calcar collars, plasma sprayed either proximally or five eighths of stem and for use with or without a PMMA cement centralizer. The devices are used to resurface the femoral hip joint and reconstitute function following the degenerative effects of osteo and rheumatoid arthritis, post trauma disease effects, avascular necrosis and septic or aseptic total hip revision. The femoral stems are manufactured from cobalt chrome alloy. The cobalt chrome plasma spray coating provides an increased surface roughness to act as key for mechanical interlock with PMMA bone cement. The stem devices may be used with any one of a range of previously cleared Corin cobalt chrome modular heads, bipolar or uni-polar modular devices. The C-Fit plasma sprayed femoral components are intended for use with bone cement only.

## SUMMARY OF SUBSTANTIAL EQUIVALENCE AND SAFETY AND EFFECTIVENESS

The C-Fit Femoral Hip system is a modification of the previously cleared V.S.P. (now called C-Fit stem) Hip system, manufactured by Corin Medical Ltd. The original V.S.P. (now called C-Fit stem) stem is manufactured from titanium alloy with a cobalt chrome plasma spray coating applied. This submission extends the range to include a cobalt chrome stem with cobalt chrome plasma spray coating and long stem options. The C-Fit cobalt chrome stem without coating is previously cleared for sale for use with cement. Corin, additionally, claims substantial equivalence to the Mallory/head system from Biomet, with the specific reference to plasma sprayed long femoral stems.

This submission is supported by extensive mechanical test data confirming the device’s safety and effectiveness. The device has been in clinical use outside the U.S. for approximately ten years and no significant post-operative problems have been reported.

---

**Source:** [https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/JDI/K965019](https://fda.innolitics.com/submissions/OR/subpart-d%E2%80%94prosthetic-devices/JDI/K965019)

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com
