FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

PUREVUE™ FMS

K Number: K250795 · Decision Dec 5, 2025
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
26
Review Days
266

Basic Information

Device Name
PUREVUE™ FMS
K Number
K250795
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
W.O.M. World of Medicine GmbH
Date Received
March 14, 2025
Decision Date
December 5, 2025
Product Code
HRX
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
HRX Arthroscope

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