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FDA 510(k)

MCCUTCHEN FEMORAL HIP PROSTHESIS

K-Number: K870174 · 1987-02-06

ApplicantDow Corning Wright
Decision Date1987-02-06
Product Code
DecisionSubstantially Equivalent

Device Summary

MCCUTCHEN FEMORAL HIP 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 1987-02-06 under 510(k) number K870174. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MCCUTCHEN FEMORAL HIP PROSTHESIS?

MCCUTCHEN FEMORAL HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1987-02-06. The listed applicant is Dow Corning Wright. The 510(k) number is K870174.

When did MCCUTCHEN FEMORAL HIP PROSTHESIS receive FDA 510(k) clearance?

MCCUTCHEN FEMORAL HIP PROSTHESIS received FDA 510(k) clearance on 1987-02-06, under 510(k) number K870174.

Who is the listed applicant for MCCUTCHEN FEMORAL HIP PROSTHESIS?

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

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Other records listing Dow Corning Wright 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.

K932210ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENTK932911ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENTK934354LACEY ALL POLYETHYLENE TIBIAL COMPONENTK932222SLT FEMORAL HEADK932858ORTHOLOC ADVANTIM TIBIAL BASE COMPONENTK930228ORTHOLOC ADVANTIM TIBIAL STEM 5 DEGREE

View all 74 devices →

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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