Browse hierarchy: [Orthopedic (OR)](/submissions/OR) → [Subpart D — Prosthetic Devices](/submissions/OR/subpart-d%E2%80%94prosthetic-devices) → [21 CFR 888.3360](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/888.3360) → JDD — Prosthesis, Upper Femoral

# JDD · Prosthesis, Upper Femoral

_Orthopedic · 21 CFR 888.3360 · Class 2_

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

## Overview

- **Product Code:** JDD
- **Device Name:** Prosthesis, Upper Femoral
- **Regulation:** [21 CFR 888.3360](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/888.3360)
- **Device Class:** 2
- **Review Panel:** [Orthopedic](/submissions/OR)
- **Implant:** yes

## Identification

A hip joint femoral (hemi-hip) metallic cemented or uncemented prosthesis is a device intended to be implanted to replace a portion of the hip joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum. This generic type of device includes designs which are intended to be fixed to the bone with bone cement (§ 888.3027) as well as designs which have large window-like holes in the stem of the device and which are intended for use without bone cement. However, in these latter designs, fixation of the device is not achieved by means of bone ingrowth.

## Classification Rationale

Class II.

## Recent Cleared Devices (0 of 0)

_No cleared devices on record._

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

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