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FDA 510(k)

THACKRAY ORTHOGENESIS IDENTIFIT FEMORAL HIP PROSTH

K-Number: K905254 · 1991-02-26

ApplicantDepuy, Inc.
Decision Date1991-02-26
Product CodeLWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

THACKRAY ORTHOGENESIS IDENTIFIT FEMORAL HIP PROSTH is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1991-02-26 under 510(k) number K905254. The device is classified under product code LWJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the THACKRAY ORTHOGENESIS IDENTIFIT FEMORAL HIP PROSTH?

THACKRAY ORTHOGENESIS IDENTIFIT FEMORAL HIP PROSTH is a medical device that received FDA 510(k) clearance on 1991-02-26. The listed applicant is Depuy, Inc.. The 510(k) number is K905254.

When did THACKRAY ORTHOGENESIS IDENTIFIT FEMORAL HIP PROSTH receive FDA 510(k) clearance?

THACKRAY ORTHOGENESIS IDENTIFIT FEMORAL HIP PROSTH received FDA 510(k) clearance on 1991-02-26, under 510(k) number K905254.

Who is the listed applicant for THACKRAY ORTHOGENESIS IDENTIFIT FEMORAL HIP PROSTH?

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

What is the FDA product code for THACKRAY ORTHOGENESIS IDENTIFIT FEMORAL HIP PROSTH?

The FDA product code for THACKRAY ORTHOGENESIS IDENTIFIT FEMORAL HIP PROSTH is LWJ.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: LWJ)

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.

K120595UNISYN PLUS HIP STEMConsensus Orthopedics, Inc.K103518TRINITY ACETABULAR SYSTEMCorin USAK090764NOVATION CFS PRESS-FIT AND CEMENTED STEMSExactech, Inc.K082146METHA SHORT STEM HIP SYSTEM XL FEMORAL HEADAesculap Implant Systems, Inc.K07006136MM COCR FEMORAL HEAD AND 36MM ACETABULAR INSERTHayes Medical, Inc.K062978U2 HIP STEM, TI PLASMA SPRAYUnited Orthopedic Corp.

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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