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

PATRIOT SPACERS

K Number: K122097 · Decision Dec 6, 2012
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
172
Review Days
143

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Basic Information

Device Name
PATRIOT SPACERS
K Number
K122097
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Globus Medical, Inc.
Date Received
July 16, 2012
Decision Date
December 6, 2012
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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K243814 NuVasive Pulse System
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