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

OCTANE STRAIGHT, OCTANE STRAIGHT - LORDOTIC, OCTANE STRAIGHT I/R, OCTANE STRAIGHT I/R - LORDOTIC

K Number: K130434 · Decision May 1, 2013
Classifications
1
FEI Numbers
422
Registration Numbers
422
Same Product Code
869
Applicant Total
146
Review Days
69

Basic Information

Device Name
OCTANE STRAIGHT, OCTANE STRAIGHT - LORDOTIC, OCTANE STRAIGHT I/R, OCTANE STRAIGHT I/R - LORDOTIC
K Number
K130434
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
EXACTECH, INC.
Date Received
February 21, 2013
Decision Date
May 1, 2013
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

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