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FDA 510(k)

P.F.C. TOTAL HIP SYSTEM

K-Number: K944132 · 1995-01-06

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1995-01-06
Product CodeKWY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

P.F.C. TOTAL HIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1995-01-06 under 510(k) number K944132. The device is classified under product code KWY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.F.C. TOTAL HIP SYSTEM?

P.F.C. TOTAL HIP SYSTEM is a medical device that received FDA 510(k) clearance on 1995-01-06. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K944132.

When did P.F.C. TOTAL HIP SYSTEM receive FDA 510(k) clearance?

P.F.C. TOTAL HIP SYSTEM received FDA 510(k) clearance on 1995-01-06, under 510(k) number K944132.

Who is the listed applicant for P.F.C. TOTAL HIP SYSTEM?

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

What is the FDA product code for P.F.C. TOTAL HIP SYSTEM?

The FDA product code for P.F.C. TOTAL HIP SYSTEM is KWY.

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Related Devices (Code: KWY)

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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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