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FDA 510(k)

PATELLAR PROSTHESIS

K-Number: K772225 · 1977-12-08

ApplicantCutter Laboratories, Inc.
Decision Date1977-12-08
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PATELLAR PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Cutter Laboratories, Inc.. It received FDA 510(k) clearance on 1977-12-08 under 510(k) number K772225. 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 PATELLAR PROSTHESIS?

PATELLAR PROSTHESIS is a medical device that received FDA 510(k) clearance on 1977-12-08. The listed applicant is Cutter Laboratories, Inc.. The 510(k) number is K772225.

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

PATELLAR PROSTHESIS received FDA 510(k) clearance on 1977-12-08, under 510(k) number K772225.

Who is the listed applicant for PATELLAR PROSTHESIS?

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

What is the FDA product code for PATELLAR PROSTHESIS?

The FDA product code for PATELLAR PROSTHESIS is 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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