Thackray Orthogenesis Identifit Femoral Hip Prosth

FDA 510(k) K905254 · Depuy, Inc.

Substantially Equivalent for Some Indications

510(k) numberK905254

Submission

Device name
Thackray Orthogenesis Identifit Femoral Hip Prosth
Applicant
Depuy, Inc.
Warsaw, IN, US
Received
November 23, 1990
Decision date
February 26, 1991
Decision
Substantially Equivalent for Some Indications (SN)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LWJ – Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3360
Specialty
Orthopedic
Implant
Yes

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K082146Metha Short Stem Hip System XL Femoral HeadLWJ · Special Aesculap Implant Systems, Inc.09/09/2008SE
K07006136MM Cocr Femoral Head and 36MM Acetabular InsertLWJ · Special Hayes Medical, Inc.01/31/2007SE
K062978U2 Hip Stem, Ti Plasma SprayLWJ · Traditional United Orthopedic Corp.01/16/2007SE
K062383Unisyn Ha Plasma Modular HipLWJ · Special Hayes Medical, Inc.12/21/2006SE
K061699ExciaLWJ · Special Aesculap, Inc.08/18/2006SE
K051826Betacone Hip Prosthesis SystemLWJ · Traditional Waldemar Link GmbH & Co. KG11/18/2005SE
K050262U2 Acetabular ComponentLWJ · Traditional United Orthopedic Corp.08/15/2005SE

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Questions and answers

When was Thackray Orthogenesis Identifit Femoral Hip Prosth cleared by the FDA?

Thackray Orthogenesis Identifit Femoral Hip Prosth (K905254) received a 510(k) decision of Substantially Equivalent for Some Indications on February 26, 1991, 95 days after the submission was received.

What is the product code of K905254?

The FDA product code is LWJ – Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented, a Class II (moderate risk) device regulated under 21 CFR 888.3360.