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

GIBRALT SPINE SYSTEMS FACET SCREW 04.0,04.5

K Number: K112097 · Decision Nov 21, 2011
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
77
Applicant Total
186
Review Days
122

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Basic Information

Device Name
GIBRALT SPINE SYSTEMS FACET SCREW 04.0,04.5
K Number
K112097
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Exactech, Inc.
Date Received
July 22, 2011
Decision Date
November 21, 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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K233482 Equinoxe® Central Screw Baseplate System
K230717 Exactech® Vantage® Total Ankle System
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K223833 Exactech® Equinoxe® Reverse Humeral Liners and Humeral Adapter Trays
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