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FDA 510(k)

THE TAPER-FIT TOTAL HIP SYSTEM

K-Number: K992234 · 1999-11-10

ApplicantCorin USA
Decision Date1999-11-10
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THE TAPER-FIT TOTAL HIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Corin USA. It received FDA 510(k) clearance on 1999-11-10 under 510(k) number K992234. 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 THE TAPER-FIT TOTAL HIP SYSTEM?

THE TAPER-FIT TOTAL HIP SYSTEM is a medical device that received FDA 510(k) clearance on 1999-11-10. The listed applicant is Corin USA. The 510(k) number is K992234.

When did THE TAPER-FIT TOTAL HIP SYSTEM receive FDA 510(k) clearance?

THE TAPER-FIT TOTAL HIP SYSTEM received FDA 510(k) clearance on 1999-11-10, under 510(k) number K992234.

Who is the listed applicant for THE TAPER-FIT TOTAL HIP SYSTEM?

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

What is the FDA product code for THE TAPER-FIT TOTAL HIP SYSTEM?

The FDA product code for THE TAPER-FIT TOTAL HIP SYSTEM is JDG.

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Other records listing Corin USA as applicant

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K203751OMNIVision systemK202805Optimized Positioning System (OPS) InsightK193545Corin Optimized Positioning System (OPS) FemoralK193042Optimized Positioning System (OPS) ReViewK192656Optimized Positioning System (OPS) InsightK190143LARS AC Band Device

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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 CompanyK962002AURA HIP SYSTEM CALCAR REPLACEMENT FEMORAL STEMExactech, Inc.K955171NEXLOCK FEMORAL STEMNexmed, 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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