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FDA 510(k)

PROXIMAL FEMORAL REPLACEMENT PROSTHESIS

K-Number: K874575 · 1988-01-07

ApplicantDow Corning Wright
Decision Date1988-01-07
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PROXIMAL FEMORAL REPLACEMENT PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Wright. It received FDA 510(k) clearance on 1988-01-07 under 510(k) number K874575. 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 PROXIMAL FEMORAL REPLACEMENT PROSTHESIS?

PROXIMAL FEMORAL REPLACEMENT PROSTHESIS is a medical device that received FDA 510(k) clearance on 1988-01-07. The listed applicant is Dow Corning Wright. The 510(k) number is K874575.

When did PROXIMAL FEMORAL REPLACEMENT PROSTHESIS receive FDA 510(k) clearance?

PROXIMAL FEMORAL REPLACEMENT PROSTHESIS received FDA 510(k) clearance on 1988-01-07, under 510(k) number K874575.

Who is the listed applicant for PROXIMAL FEMORAL REPLACEMENT PROSTHESIS?

The FDA 510(k) record lists Dow Corning Wright as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROXIMAL FEMORAL REPLACEMENT PROSTHESIS?

The FDA product code for PROXIMAL FEMORAL REPLACEMENT PROSTHESIS is JDG.

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Other records listing Dow Corning Wright as applicant

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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

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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