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

PIONEER INTERVERTEBRAL FUSION DEVICE SYSTEM

K Number: K073177 · Decision May 13, 2008
Classifications
1
FEI Numbers
422
Registration Numbers
422
Same Product Code
869
Applicant Total
50
Review Days
182

Basic Information

Device Name
PIONEER INTERVERTEBRAL FUSION DEVICE SYSTEM
K Number
K073177
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PIONEER SURGICAL TECHNOLOGY
Date Received
November 13, 2007
Decision Date
May 13, 2008
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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