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FDA 510(k)

P.F.C. HIP SYSTEM POROUS COATED FEMORAL COMPONENT

K-Number: K893872 · 1989-09-11

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1989-09-11
Product CodeKWY
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

P.F.C. HIP SYSTEM POROUS COATED FEMORAL COMPONENT 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 1989-09-11 under 510(k) number K893872. The device is classified under product code KWY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the P.F.C. HIP SYSTEM POROUS COATED FEMORAL COMPONENT?

P.F.C. HIP SYSTEM POROUS COATED FEMORAL COMPONENT is a medical device that received FDA 510(k) clearance on 1989-09-11. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K893872.

When did P.F.C. HIP SYSTEM POROUS COATED FEMORAL COMPONENT receive FDA 510(k) clearance?

P.F.C. HIP SYSTEM POROUS COATED FEMORAL COMPONENT received FDA 510(k) clearance on 1989-09-11, under 510(k) number K893872.

Who is the listed applicant for P.F.C. HIP SYSTEM POROUS COATED FEMORAL COMPONENT?

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. HIP SYSTEM POROUS COATED FEMORAL COMPONENT?

The FDA product code for P.F.C. HIP SYSTEM POROUS COATED FEMORAL COMPONENT is KWY.

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Related Devices (Code: KWY)

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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