FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

TRYPTIK2C-plate Anterior Cervical Plate System

K Number: K153042 · Decision Mar 28, 2016
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
655
Applicant Total
32
Review Days
161

Basic Information

Device Name
TRYPTIK2C-plate Anterior Cervical Plate System
K Number
K153042
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SPINEART
Date Received
October 19, 2015
Decision Date
March 28, 2016
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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