FDA 510(k)

PROSTHESIS, TOTAL HIP-FEMORAL

K-Number: K760106 · 1976-07-20

Decision Date1976-07-20

Product CodeJDG

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

PROSTHESIS, TOTAL HIP-FEMORAL is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760106. The device is classified under product code JDG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROSTHESIS, TOTAL HIP-FEMORAL?

PROSTHESIS, TOTAL HIP-FEMORAL is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K760106.

When did PROSTHESIS, TOTAL HIP-FEMORAL receive FDA 510(k) clearance?

PROSTHESIS, TOTAL HIP-FEMORAL received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760106.

Who is the listed applicant for PROSTHESIS, TOTAL HIP-FEMORAL?

The FDA 510(k) record lists Orthopedic Equipment Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROSTHESIS, TOTAL HIP-FEMORAL?

The FDA product code for PROSTHESIS, TOTAL HIP-FEMORAL is JDG.

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Other records listing Orthopedic Equipment Co., Inc. as applicant

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Related Devices (Code: JDG)

K212431Biomet Answer/Impact/Integral Distal Centralizer/Centering SleeveBiomet, Inc.K193546Distal CentralizersBiomet, Inc.K173499Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral HeadsStryker Orthopaedics K001984PROGENY FORGED COCR CEMENTED FEMORAL COMPONENTStelkast Company K992234THE TAPER-FIT TOTAL HIP SYSTEMCorin USA K962002AURA HIP SYSTEM CALCAR REPLACEMENT FEMORAL STEMExactech, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.