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

CORRIDOR Fixation System

K Number: K192744 · Decision Dec 16, 2019
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
77
Applicant Total
172
Review Days
77

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Basic Information

Device Name
CORRIDOR Fixation System
K Number
K192744
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Globus Medical, Inc.
Date Received
September 30, 2019
Decision Date
December 16, 2019
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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