Metha Short Stem Hip System XL Femoral Head

FDA 510(k) K082146 · Aesculap Implant Systems, Inc.

Substantially Equivalent

510(k) numberK082146

Submission

Device name
Metha Short Stem Hip System XL Femoral Head
Applicant
Aesculap Implant Systems, Inc.
Center Valley, PA, US
Received
July 30, 2008
Decision date
September 9, 2008
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

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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K120595Unisyn Plus Hip StemLWJ · Traditional Consensus Orthopedics, Inc.10/12/2012SE
K103518Trinity Acetabular SystemLWJ · Traditional Corin USA03/09/2011SE
K090764Novation CFS Press-Fit and Cemented StemsLWJ · Special Exactech, Inc.04/21/2009SE
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
K042344Excia Total Hip SystemLWJ · Abbreviated Aesculap, Inc.03/16/2005SE

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Questions and answers

When was Metha Short Stem Hip System XL Femoral Head cleared by the FDA?

Metha Short Stem Hip System XL Femoral Head (K082146) received a 510(k) decision of Substantially Equivalent on September 9, 2008, 41 days after the submission was received.

What is the product code of K082146?

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.