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FDA 510(k)

WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO

K-Number: K874740 · 1987-12-18

ApplicantDow Corning Wright
Decision Date1987-12-18
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO 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 1987-12-18 under 510(k) number K874740. The device is classified under product code JDG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO?

WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO is a medical device that received FDA 510(k) clearance on 1987-12-18. The listed applicant is Dow Corning Wright. The 510(k) number is K874740.

When did WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO receive FDA 510(k) clearance?

WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO received FDA 510(k) clearance on 1987-12-18, under 510(k) number K874740.

Who is the listed applicant for WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO?

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 WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO?

The FDA product code for WHITESIDE ORTHOLOC CALCAR REPLACEMENT HIP STEM PRO is JDG.

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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

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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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