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

CMORE® CT System; CMORE® CT System Navigated Instruments

K Number: K252327 · Decision Nov 12, 2025
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
117
Applicant Total
16
Review Days
110

Basic Information

Device Name
CMORE® CT System; CMORE® CT System Navigated Instruments
K Number
K252327
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3075
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Icotec AG
Date Received
July 25, 2025
Decision Date
November 12, 2025
Product Code
NKG
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
NKG Posterior Cervical Screw System

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