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

FUSION ADVANTAGE CERVICAL CAGE, FUSION ADVANTAGE LUMBAR CAGE

K Number: K083425 · Decision Mar 20, 2009
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
2
Review Days
121

Basic Information

Device Name
FUSION ADVANTAGE CERVICAL CAGE, FUSION ADVANTAGE LUMBAR CAGE
K Number
K083425
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Adaptive Specialty, LLC
Date Received
November 19, 2008
Decision Date
March 20, 2009
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

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K Number Device Name
K110662 ADAPTIVE WEDGE