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

Pyrenees Cervical Plate System

K Number: K153526 · Decision Apr 27, 2016
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
16
Review Days
140

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Basic Information

Device Name
Pyrenees Cervical Plate System
K Number
K153526
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
K2m
Date Received
December 9, 2015
Decision Date
April 27, 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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