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FDA 510(k)

P.F.C. TOTAL KNEE SYSTEM OVAL PATELLA

K-Number: K935262 · 1994-06-03

ApplicantJohnson & Johnson Orthopaedics, Inc.
Decision Date1994-06-03
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

P.F.C. TOTAL KNEE SYSTEM OVAL PATELLA is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Orthopaedics, Inc.. It received FDA 510(k) clearance on 1994-06-03 under 510(k) number K935262. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the P.F.C. TOTAL KNEE SYSTEM OVAL PATELLA?

P.F.C. TOTAL KNEE SYSTEM OVAL PATELLA is a medical device that received FDA 510(k) clearance on 1994-06-03. The listed applicant is Johnson & Johnson Orthopaedics, Inc.. The 510(k) number is K935262.

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

P.F.C. TOTAL KNEE SYSTEM OVAL PATELLA received FDA 510(k) clearance on 1994-06-03, under 510(k) number K935262.

Who is the listed applicant for P.F.C. TOTAL KNEE SYSTEM OVAL PATELLA?

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

What is the FDA product code for P.F.C. TOTAL KNEE SYSTEM OVAL PATELLA?

The FDA product code for P.F.C. TOTAL KNEE SYSTEM OVAL PATELLA is JWH.

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Other records listing Johnson & Johnson Orthopaedics, Inc. as applicant

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.

K931466PFC MODULAR TOTAL KNEE SYSTEM, POROUS COATED SACRIK935452P.F.C. 2 TOTAL HIP SYSTEM POROUS COATED MODULAR FEMORAL COMPONENTK940190ULTIMA UNIPOLAR MODULAR HEADK933275P.F.C. CERAMIC HIP HEADK932595ORTHOSORB(TM) ABSORBABLE CEMENT RESTRICTORK931655P.F.C. BIPOLAR HIP SYSTEM

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Related Devices (Code: JWH)

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.

K262057GMK ExtensionMedacta International SAK260063GSPE SpacerThe General Hospital Corporation, d/b/a MassachusettsK262293EVOLUTION MPX™ Total Knee SystemSuzhou Microport Orthorecon Co., Ltd.K262341b-ONE® Mobio™ Total Knee System Revision Cemented Tibial Augments, Stem Extensions and Press-Fit Stem ExtensionsB-One Ortho, Corp.K262130ATTUNE Revision Knee SystemDepuy Orthopaedics, Inc.K253961SK Knee SystemJust Medical Devices (Tianjin) Co., Ltd.

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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