FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

SPARTAN S3 FACET SYSTEM

K Number: K113011 · Decision Dec 6, 2011
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
77
Applicant Total
16
Review Days
56

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Basic Information

Device Name
SPARTAN S3 FACET SYSTEM
K Number
K113011
Device Class
FDA unclassified
Clearance Type
Special
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Amendia, Inc.
Date Received
October 11, 2011
Decision Date
December 6, 2011
Product Code
MRW
Advisory Committee
Unknown
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
MRW System, Facet Screw Spinal Device

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