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FDA 510(k)

PROSTHESIS, PATELLAR ARTICULAR SURFACE

K-Number: K760200 · 1976-07-20

ApplicantDepuy, Inc.
Decision Date1976-07-20
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PROSTHESIS, PATELLAR ARTICULAR SURFACE is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760200. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROSTHESIS, PATELLAR ARTICULAR SURFACE?

PROSTHESIS, PATELLAR ARTICULAR SURFACE is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Depuy, Inc.. The 510(k) number is K760200.

When did PROSTHESIS, PATELLAR ARTICULAR SURFACE receive FDA 510(k) clearance?

PROSTHESIS, PATELLAR ARTICULAR SURFACE received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760200.

Who is the listed applicant for PROSTHESIS, PATELLAR ARTICULAR SURFACE?

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

What is the FDA product code for PROSTHESIS, PATELLAR ARTICULAR SURFACE?

The FDA product code for PROSTHESIS, PATELLAR ARTICULAR SURFACE is JWH.

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Related Devices (Code: JWH)

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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.

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