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FDA 510(k)

NEXLOCK FEMORAL STEM

K-Number: K955171 · 1996-02-09

ApplicantNexmed, Inc.
Decision Date1996-02-09
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NEXLOCK FEMORAL STEM is the device name listed in this FDA 510(k) record. The listed applicant is Nexmed, Inc.. It received FDA 510(k) clearance on 1996-02-09 under 510(k) number K955171. The device is classified under product code JDG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEXLOCK FEMORAL STEM?

NEXLOCK FEMORAL STEM is a medical device that received FDA 510(k) clearance on 1996-02-09. The listed applicant is Nexmed, Inc.. The 510(k) number is K955171.

When did NEXLOCK FEMORAL STEM receive FDA 510(k) clearance?

NEXLOCK FEMORAL STEM received FDA 510(k) clearance on 1996-02-09, under 510(k) number K955171.

Who is the listed applicant for NEXLOCK FEMORAL STEM?

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

What is the FDA product code for NEXLOCK FEMORAL STEM?

The FDA product code for NEXLOCK FEMORAL STEM is JDG.

Related Clinical Trials

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.

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Other records listing Nexmed, 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.

K033580NEXFLEX TOTAL HIP SYSTEMK991882NEXFLEX TOTAL KNEE SYSTEMK955170NEXFLEX FEMORAL STEM, STANDARD DESIGNK952629NEXFLEX TOTAL HIP SYSTEMK951656NEXMED CANCELLOUS BONE SCREWS

Related Devices (Code: JDG)

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.

K212431Biomet Answer/Impact/Integral Distal Centralizer/Centering SleeveBiomet, Inc.K193546Distal CentralizersBiomet, Inc.K173499Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral HeadsStryker OrthopaedicsK001984PROGENY FORGED COCR CEMENTED FEMORAL COMPONENTStelkast CompanyK992234THE TAPER-FIT TOTAL HIP SYSTEMCorin USAK962002AURA HIP SYSTEM CALCAR REPLACEMENT FEMORAL STEMExactech, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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