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FDA 510(k)

CHARNLEY REVISION SET

K-Number: K760976 · 1976-11-16

ApplicantCodman & Shurtleff, Inc.
Decision Date1976-11-16
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CHARNLEY REVISION SET is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1976-11-16 under 510(k) number K760976. 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 CHARNLEY REVISION SET?

CHARNLEY REVISION SET is a medical device that received FDA 510(k) clearance on 1976-11-16. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K760976.

When did CHARNLEY REVISION SET receive FDA 510(k) clearance?

CHARNLEY REVISION SET received FDA 510(k) clearance on 1976-11-16, under 510(k) number K760976.

Who is the listed applicant for CHARNLEY REVISION SET?

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

What is the FDA product code for CHARNLEY REVISION SET?

The FDA product code for CHARNLEY REVISION SET is JDG.

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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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