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

O-arm O2 Imaging System

K Number: K200074 · Decision Apr 24, 2020
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
209
Review Days
101

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Basic Information

Device Name
O-arm O2 Imaging System
K Number
K200074
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic, Inc.
Date Received
January 14, 2020
Decision Date
April 24, 2020
Product Code
OWB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OWB Interventional Fluoroscopic X-Ray System

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