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FDA 510(k)

CONSENSUS HIP SYSTEM- NON-POROUS TITANIUM FEMORAL STEM

K-Number: K933499 · 1994-05-18

ApplicantU.S. Medical Products, Inc.
Decision Date1994-05-18
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONSENSUS HIP SYSTEM- NON-POROUS TITANIUM FEMORAL STEM is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Medical Products, Inc.. It received FDA 510(k) clearance on 1994-05-18 under 510(k) number K933499. 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 CONSENSUS HIP SYSTEM- NON-POROUS TITANIUM FEMORAL STEM?

CONSENSUS HIP SYSTEM- NON-POROUS TITANIUM FEMORAL STEM is a medical device that received FDA 510(k) clearance on 1994-05-18. The listed applicant is U.S. Medical Products, Inc.. The 510(k) number is K933499.

When did CONSENSUS HIP SYSTEM- NON-POROUS TITANIUM FEMORAL STEM receive FDA 510(k) clearance?

CONSENSUS HIP SYSTEM- NON-POROUS TITANIUM FEMORAL STEM received FDA 510(k) clearance on 1994-05-18, under 510(k) number K933499.

Who is the listed applicant for CONSENSUS HIP SYSTEM- NON-POROUS TITANIUM FEMORAL STEM?

The FDA 510(k) record lists U.S. Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONSENSUS HIP SYSTEM- NON-POROUS TITANIUM FEMORAL STEM?

The FDA product code for CONSENSUS HIP SYSTEM- NON-POROUS TITANIUM FEMORAL STEM is LZO.

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Other records listing U.S. Medical Products, 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.

K962215CONSENSUS POSTERIOR STABILIZED KNEE-INTERCONDYLAR NOTCH ROUTERK954818CONSENSUS POSTERIOR STABILIZED KNEEK953443CONSENSUS PCL SUBSITUTING TIBIAL INSERTK952943CONSENSUS ALL POLY TIBIAK960302CONSENSUS ACETABULAR SHELL, ALL UHMWPEK960340CONSENSUS APEX DOME HOLE PLUG

View all 24 devices →

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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