FDA 510(k) FDA class 2 Substantially Equivalent 🇧🇪 Belgium

ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM, ZIMMER PATIENT SPECIFIC INSTRUMENTS, ZIMMER PATIENT SPECIFIC INSTRUMENTS PLA

K Number: K133162 · Decision Feb 25, 2014
Classifications
1
FEI Numbers
320
Registration Numbers
320
Same Product Code
902
Applicant Total
26
Review Days
131

Basic Information

Device Name
ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM, ZIMMER PATIENT SPECIFIC INSTRUMENTS, ZIMMER PATIENT SPECIFIC INSTRUMENTS PLA
K Number
K133162
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MATERIALISE N.V.
Date Received
October 17, 2013
Decision Date
February 25, 2014
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

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K Number Device Name
K150928 Materialise TKA Guide System, Materialise TKA Planner, Materialise TKA Guides
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K132290 SURGICASE ORTHOPAEDICS SYSTEM, SURGICASE CONNECT, SURGICASE GUIDES
K140257 SIGNATURE PLANNER, SIGNATURE GUIDES
K131559 MATCH POINT SYSTEM(TM), SURGICASE CONNECT, MATCH POINT SYSTEM(TM) GUIDES
K121640 ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM
K112389 SURGICASE CONNECT, SURGICASE GUIDE
K111863 SIGNATURE PLANNER,SIGNATURE GUIDES
K113599 SURGICASE CONNECT
K113829 ZIMMER PATIENT SPECIFIC INSTRUMENT SYSTEM ZIMMER PATIENT SPECIFIC INSTRUMENTS ZIMMER PATIENT SPECIFIC INSTRUMENTS PLANNE
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