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

SurgTech Thoracolumbosacral (TLS) Posterior Fixation System

K Number: K163363 · Decision Apr 5, 2017
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
6
Review Days
126

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Basic Information

Device Name
SurgTech Thoracolumbosacral (TLS) Posterior Fixation System
K Number
K163363
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Surgtech, Inc.
Date Received
November 30, 2016
Decision Date
April 5, 2017
Product Code
NKB
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
NKB Thoracolumbosacral Pedicle Screw System

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