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FDA 510(k)

AML CALCAR FEMORAL PROSTHESIS

K-Number: K874100 · 1987-12-31

ApplicantDepuy, Inc.
Decision Date1987-12-31
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

AML CALCAR FEMORAL PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1987-12-31 under 510(k) number K874100. The device is classified under product code JDG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the AML CALCAR FEMORAL PROSTHESIS?

AML CALCAR FEMORAL PROSTHESIS is a medical device that received FDA 510(k) clearance on 1987-12-31. The listed applicant is Depuy, Inc.. The 510(k) number is K874100.

When did AML CALCAR FEMORAL PROSTHESIS receive FDA 510(k) clearance?

AML CALCAR FEMORAL PROSTHESIS received FDA 510(k) clearance on 1987-12-31, under 510(k) number K874100.

Who is the listed applicant for AML CALCAR FEMORAL PROSTHESIS?

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 AML CALCAR FEMORAL PROSTHESIS?

The FDA product code for AML CALCAR FEMORAL PROSTHESIS 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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