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

TiWAVE-C™ Porous Titanium Cervical Cage

K Number: K180401 · Decision Jun 14, 2018
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
9
Review Days
120

Basic Information

Device Name
TiWAVE-C™ Porous Titanium Cervical Cage
K Number
K180401
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kalitec Direct, LLC
Date Received
February 14, 2018
Decision Date
June 14, 2018
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

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