FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

NAVIO™ Surgical System (NAVIO system)

K Number: K180271 · Decision Apr 6, 2018
Classifications
1
FEI Numbers
370
Registration Numbers
370
Same Product Code
404
Applicant Total
15
Review Days
65

Basic Information

Device Name
NAVIO™ Surgical System (NAVIO system)
K Number
K180271
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Blue Belt Technologies, Inc.
Date Received
January 31, 2018
Decision Date
April 6, 2018
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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