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

MATCH POINT SYSTEM(TM), SURGICASE CONNECT, MATCH POINT SYSTEM(TM) GUIDES

K Number: K131559 · Decision Sep 27, 2013
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
186
Applicant Total
26
Review Days
120

Basic Information

Device Name
MATCH POINT SYSTEM(TM), SURGICASE CONNECT, MATCH POINT SYSTEM(TM) GUIDES
K Number
K131559
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3660
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MATERIALISE N.V.
Date Received
May 30, 2013
Decision Date
September 27, 2013
Product Code
KWS
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
KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

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K132290 SURGICASE ORTHOPAEDICS SYSTEM, SURGICASE CONNECT, SURGICASE GUIDES
K140257 SIGNATURE PLANNER, SIGNATURE GUIDES
K133162 ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM, ZIMMER PATIENT SPECIFIC INSTRUMENTS, ZIMMER PATIENT SPECIFIC INSTRUMENTS PLA
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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