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FDA 510(k)

P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUS

K-Number: K923807 · 1992-11-09

ApplicantJohnson & Johnson International
Decision Date1992-11-09
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson International. It received FDA 510(k) clearance on 1992-11-09 under 510(k) number K923807. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUS?

P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUS is a medical device that received FDA 510(k) clearance on 1992-11-09. The listed applicant is Johnson & Johnson International. The 510(k) number is K923807.

When did P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUS receive FDA 510(k) clearance?

P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUS received FDA 510(k) clearance on 1992-11-09, under 510(k) number K923807.

Who is the listed applicant for P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUS?

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

What is the FDA product code for P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUS?

The FDA product code for P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUS is JWH.

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Other records listing Johnson & Johnson International as applicant

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Related Devices (Code: JWH)

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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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