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

Precision Spine Navigation Instrumentation

K Number: K181606 · Decision Sep 27, 2019
Classifications
1
FEI Numbers
370
Registration Numbers
370
Same Product Code
404
Applicant Total
16
Review Days
465

Basic Information

Device Name
Precision Spine Navigation Instrumentation
K Number
K181606
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Precision Spine, Inc.
Date Received
June 19, 2018
Decision Date
September 27, 2019
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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K172495 Reform® POCT System
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