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FDA 510(k)

CHARNLEY FEMORAL COMPONENT

K-Number: K760974 · 1976-11-16

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

Device Summary

CHARNLEY FEMORAL COMPONENT 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 K760974. 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 FEMORAL COMPONENT?

CHARNLEY FEMORAL COMPONENT 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 K760974.

When did CHARNLEY FEMORAL COMPONENT receive FDA 510(k) clearance?

CHARNLEY FEMORAL COMPONENT received FDA 510(k) clearance on 1976-11-16, under 510(k) number K760974.

Who is the listed applicant for CHARNLEY FEMORAL COMPONENT?

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 FEMORAL COMPONENT?

The FDA product code for CHARNLEY FEMORAL COMPONENT is JDG.

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Related Devices (Code: JDG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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