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FDA 510(k)

P.C.A. TOTAL HIP FEMORAL COMPONENT MODIFICATION

K-Number: K852964 · 1985-07-29

ApplicantHowmedica Corp.
Decision Date1985-07-29
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

P.C.A. TOTAL HIP FEMORAL COMPONENT MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1985-07-29 under 510(k) number K852964. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.C.A. TOTAL HIP FEMORAL COMPONENT MODIFICATION?

P.C.A. TOTAL HIP FEMORAL COMPONENT MODIFICATION is a medical device that received FDA 510(k) clearance on 1985-07-29. The listed applicant is Howmedica Corp.. The 510(k) number is K852964.

When did P.C.A. TOTAL HIP FEMORAL COMPONENT MODIFICATION receive FDA 510(k) clearance?

P.C.A. TOTAL HIP FEMORAL COMPONENT MODIFICATION received FDA 510(k) clearance on 1985-07-29, under 510(k) number K852964.

Who is the listed applicant for P.C.A. TOTAL HIP FEMORAL COMPONENT MODIFICATION?

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

What is the FDA product code for P.C.A. TOTAL HIP FEMORAL COMPONENT MODIFICATION?

The FDA product code for P.C.A. TOTAL HIP FEMORAL COMPONENT MODIFICATION is DXQ.

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Related Devices (Code: DXQ)

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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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