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

STRYKER SPINE AVS PL PEEK SPACERS

K Number: K082014 · Decision Jul 28, 2008
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
124
Review Days
13

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Basic Information

Device Name
STRYKER SPINE AVS PL PEEK SPACERS
K Number
K082014
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Corp.
Date Received
July 15, 2008
Decision Date
July 28, 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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