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

SPINAL USA ANTERIOR CERVICAL INTERBODY FUSION DEVICE

K Number: K083118 · Decision May 27, 2009
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
23
Review Days
217

Basic Information

Device Name
SPINAL USA ANTERIOR CERVICAL INTERBODY FUSION DEVICE
K Number
K083118
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spinal USA
Date Received
October 22, 2008
Decision Date
May 27, 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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