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

CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays

K Number: K241893 · Decision Sep 16, 2024
Classifications
1
FEI Numbers
370
Registration Numbers
370
Same Product Code
404
Applicant Total
43
Review Days
80

Basic Information

Device Name
CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays
K Number
K241893
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medos International SARL
Date Received
June 28, 2024
Decision Date
September 16, 2024
Product Code
OLO
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
OLO Orthopedic Stereotaxic Instrument

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