Cleared Special

K103189 - MEDACTA TOTAL HIP PROSTHESIS SYSTEM - AMISTEM C & QUADRA C SHORT NECK (FDA 510(k) Clearance)

Dec 2010
Decision
53d
Days
Class 2
Risk

K103189 is an FDA 510(k) clearance for the MEDACTA TOTAL HIP PROSTHESIS SYSTEM - AMISTEM C & QUADRA C SHORT NECK. This device is classified as a Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented (Class II - Special Controls, product code LZO).

Submitted by Medacta International S.A. (San Diego, US). The FDA issued a Cleared decision on December 20, 2010, 53 days after receiving the submission on October 28, 2010.

This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3353.

Submission Details

510(k) Number K103189 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 28, 2010
Decision Date December 20, 2010
Days to Decision 53 days
Submission Type Special
Review Panel Orthopedic (OR)
Summary Summary PDF

Device Classification

Product Code LZO — Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented
Device Class Class II - Special Controls
CFR Regulation 21 CFR 888.3353

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