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FDA 510(k)

P.F.C. CRUCIATE RETAING KNEE SYSTEM

K-Number: K963117 · 1996-11-06

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1996-11-06
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

P.F.C. CRUCIATE RETAING KNEE 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 1996-11-06 under 510(k) number K963117. 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. CRUCIATE RETAING KNEE SYSTEM?

P.F.C. CRUCIATE RETAING KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 1996-11-06. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K963117.

When did P.F.C. CRUCIATE RETAING KNEE SYSTEM receive FDA 510(k) clearance?

P.F.C. CRUCIATE RETAING KNEE SYSTEM received FDA 510(k) clearance on 1996-11-06, under 510(k) number K963117.

Who is the listed applicant for P.F.C. CRUCIATE RETAING KNEE 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. CRUCIATE RETAING KNEE SYSTEM?

The FDA product code for P.F.C. CRUCIATE RETAING KNEE SYSTEM is JWH.

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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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