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

O-arm O2 Imaging System

K Number: K240465 · Decision Jun 21, 2024
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
35
Review Days
126

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Basic Information

Device Name
O-arm O2 Imaging System
K Number
K240465
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Navigation, Inc.
Date Received
February 16, 2024
Decision Date
June 21, 2024
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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K231976 StealthStation Cranial Software, v3.1.5 (9735585)
K221087 Synergy Cranial v2.2.9, StealthStation Cranial v3.1.4
K211269 Visualase MRI-Guided Laser Ablation System (SW 3.4)
K203639 StealthStation Cranial Software v1.3.2
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