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

TRUSS THORACOLUMBAR PLATE SYSTEM

K Number: K092108 · Decision Aug 13, 2009
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
172
Review Days
30

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
TRUSS THORACOLUMBAR PLATE SYSTEM
K Number
K092108
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Globus Medical, Inc.
Date Received
July 14, 2009
Decision Date
August 13, 2009
Product Code
KWQ
Advisory Committee
Orthopedic
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KWQ), ordered by most recent decision date.

View all

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. →