FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

TRANSITION STABILIZATION SYSTEM

K Number: K073439 · Decision Feb 20, 2009
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
21
Applicant Total
172
Review Days
441

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Basic Information

Device Name
TRANSITION STABILIZATION SYSTEM
K Number
K073439
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Unknown
Statement or Summary
Summary
Applicant
Globus Medical, Inc.
Date Received
December 7, 2007
Decision Date
February 20, 2009
Product Code
NQP
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
NQP Posterior Metal/Polymer Spinal System, Fusion

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K250599 ExcelsiusGPS™ Instruments
K251161 ANTHEM® Fracture System
K241525 ExcelsiusXR™
K243456 ONVOY™ Acetabular System
K243814 NuVasive Pulse System
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