FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

Zimmer Hip Joint Replacement

K Number: K200112 · Decision Apr 10, 2020
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
43
Review Days
84

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Basic Information

Device Name
Zimmer Hip Joint Replacement
K Number
K200112
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zimmer GmbH
Date Received
January 17, 2020
Decision Date
April 10, 2020
Product Code
LZO
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

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K193030 Avenir Muller Stem, Avenir Cemented Hip Stem
K192236 Fitmore Hip Stem
K192312 Zimmer Natural Nail System Cephalomedullary Nails
K192416 BIOLOX Delta Ceramic Femoral Heads, BIOLOX Option Ceramic Femoral Head System
K192217 NCB Plating System Distal Femur and Proximal Tibia
K192021 NCB Polyaxial Locking Plate System
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