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

TirboLOX-C Cervical IBFD

K Number: K181229 · Decision Sep 19, 2018
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
8
Review Days
133

Basic Information

Device Name
TirboLOX-C Cervical IBFD
K Number
K181229
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Captiva Spine, Inc.
Date Received
May 9, 2018
Decision Date
September 19, 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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K Number Device Name
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K120292 CAPLOX II PEDICLE SCREW SYSTEM
K111115 CAPTIVA SPINE CAPLOX II SPINAL FIXATION SYSTEM
K110585 CAPTIVA SPINE FUSELOX CERVICAL CAGE
K092017 PIVOTEC LUMBAR INTERBODY FUSION DEVICE (LIFD)