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

BRIDALVEIL Occipital Cervical Thoracic System

K Number: K171250 · Decision Oct 2, 2017
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
117
Applicant Total
21
Review Days
157

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Basic Information

Device Name
BRIDALVEIL Occipital Cervical Thoracic System
K Number
K171250
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3075
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Astura Medical
Date Received
April 28, 2017
Decision Date
October 2, 2017
Product Code
NKG
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
NKG Posterior Cervical Screw System

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