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

Excelsius3D

K Number: K210912 · Decision Aug 12, 2021
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
172
Review Days
136

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Basic Information

Device Name
Excelsius3D
K Number
K210912
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Globus Medical, Inc.
Date Received
March 29, 2021
Decision Date
August 12, 2021
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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Other Clearances by Globus Medical, Inc.

K Number Device Name
K253739 SCRIPT™ Rods, CREO™ Stabilization System, REVERE® Stabilization System, REVERE® 4.5 Stabilization System, NuVasive Reline™ System
K253401 SCRIPT™ Implant System
K261043 AUTOBAHN™ Nailing System
K252166 RIB LINK™ Fixation System
K253876 HEDRON™ Cervical Spacers (HEDRON C-MIS™ Spacer)
K250599 ExcelsiusGPS™ Instruments
K251161 ANTHEM® Fracture System
K241525 ExcelsiusXR™
K243456 ONVOY™ Acetabular System
K243814 NuVasive Pulse System
Search all 172 clearances from Globus Medical, Inc. →