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

V3 Segmental Plating System

K Number: K182418 · Decision Nov 29, 2018
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
15
Review Days
85

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Basic Information

Device Name
V3 Segmental Plating System
K Number
K182418
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Atlas Spine, Inc.
Date Received
September 5, 2018
Decision Date
November 29, 2018
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

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