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

TiGer Shark™ System

K Number: K172816 · Decision Jan 26, 2018
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
22
Review Days
130

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Basic Information

Device Name
TiGer Shark™ System
K Number
K172816
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Choicespine, LP
Date Received
September 18, 2017
Decision Date
January 26, 2018
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

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