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FDA 510(k)

P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR

K-Number: K930712 · 1993-10-04

ApplicantJohnson & Johnson Orthopaedics, Inc.
Decision Date1993-10-04
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR 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 1993-10-04 under 510(k) number K930712. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR?

P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR is a medical device that received FDA 510(k) clearance on 1993-10-04. The listed applicant is Johnson & Johnson Orthopaedics, Inc.. The 510(k) number is K930712.

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

P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR received FDA 510(k) clearance on 1993-10-04, under 510(k) number K930712.

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

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 HIP SYSTEM POROUS COATED MODULAR?

The FDA product code for P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR is LZO.

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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: LZO)

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.

K260173M-Vizion Femoral Revision System ExtensionMedacta International S.A.K253948Momentum Acetabular Cup SystemUnited Orthopedic CorporationK261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast GmbH

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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