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

CAVUX™ Cervical Cage

K Number: K161642 · Decision Oct 7, 2016
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
21
Review Days
115

Basic Information

Device Name
CAVUX™ Cervical Cage
K Number
K161642
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Providence Medical Technology, Inc.
Date Received
June 14, 2016
Decision Date
October 7, 2016
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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Other Clearances by Providence Medical Technology, Inc.

K Number Device Name
K261665 CORUS™ Navigation System-GN
K253676 CORUS™ Posterior Cervical Stabilization System 3D (CORUS™ PCSS 3D)
K253190 CORUS-LX Implant
K251060 CORUS™ Navigation System-GX
K251885 CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant
K241035 PMT Posterior Cervical Stabilization System (PCSS)
K240625 CORUS Navigation Access System
K230840 PMT Facet Fixation System, Lumbar (PMT FFS-LX)
K230297 PMT Expandable Cage (PMT EXP)
K220951 PMT Facet Fixation System (PMT FFS)
Search all 21 clearances from Providence Medical Technology, Inc. →