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

NextAR(TM) Shoulder Platform

K Number: K251737 · Decision Sep 4, 2025
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
41
Applicant Total
165
Review Days
90

Basic Information

Device Name
NextAR(TM) Shoulder Platform
K Number
K251737
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medacta International S.A.
Date Received
June 6, 2025
Decision Date
September 4, 2025
Product Code
SBF
Advisory Committee
Neurology
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
SBF Orthopedic Augmented Reality

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