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FDA 510(k)

CONSENSUS 32MM COCRMO FEMORAL HEAD

K-Number: K960156 · 1996-02-21

ApplicantU.S. Medical Products, Inc.
Decision Date1996-02-21
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONSENSUS 32MM COCRMO FEMORAL HEAD 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 1996-02-21 under 510(k) number K960156. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONSENSUS 32MM COCRMO FEMORAL HEAD?

CONSENSUS 32MM COCRMO FEMORAL HEAD is a medical device that received FDA 510(k) clearance on 1996-02-21. The listed applicant is U.S. Medical Products, Inc.. The 510(k) number is K960156.

When did CONSENSUS 32MM COCRMO FEMORAL HEAD receive FDA 510(k) clearance?

CONSENSUS 32MM COCRMO FEMORAL HEAD received FDA 510(k) clearance on 1996-02-21, under 510(k) number K960156.

Who is the listed applicant for CONSENSUS 32MM COCRMO FEMORAL HEAD?

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 32MM COCRMO FEMORAL HEAD?

The FDA product code for CONSENSUS 32MM COCRMO FEMORAL HEAD is JDI.

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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 INSERTK960302CONSENSUS ACETABULAR SHELL, ALL UHMWPEK952943CONSENSUS ALL POLY TIBIAK960340CONSENSUS APEX DOME HOLE PLUG

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Related Devices (Code: JDI)

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.

K253515Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and AugmentsBiomet Orthopedics, Inc.K253434OSSTM Orthopedic Salvage SystemBiomet, Inc.K243571Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained LinersZimmer BiometK240783Anthology Hip Stems; CPCS Hip Stems; Femoral Heads; R3 Acetabular Liners; Spectron Hip Stems; Synergy Hip StemsSmith & Nephew, Inc.K241716Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee ComponentHowmedica Osteonics Corp., Dba Stryker OrthopaedicsK240418Stryker Orthopaedics Hip Systems Labeling UpdateHowmedica Osteonics Corp., Dba Stryker Orthopaedics

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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