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

Materialise TKA Guide System

K Number: K251554 · Decision Jul 14, 2025
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
61
Review Days
54

Basic Information

Device Name
Materialise TKA Guide System
K Number
K251554
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Materialise NV
Date Received
May 21, 2025
Decision Date
July 14, 2025
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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