510(k) K253793

Device
Materialise TKA Guide System
Applicant
Materialise NV
510(k) number
K253793
Product code
JWH
Decision
Substantially Equivalent (SESE)
Decision date
2026-01-06
Date received
2025-11-28
Regulation
888.3560
Classification name
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Giulia Girola
Address
Technologielaan 15 Leuven BE 3001 3001

FDA Registration Numbers

Source Documents

510(k) summary PDF

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