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

FacetBRIDGE System

K Number: K152137 · Decision Jan 25, 2016
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
77
Applicant Total
25
Review Days
178

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Basic Information

Device Name
FacetBRIDGE System
K Number
K152137
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ldr Spine USA
Date Received
July 31, 2015
Decision Date
January 25, 2016
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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