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

ZAVATION IBF SYSTEMS

K Number: K112664 · Decision Dec 23, 2011
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
15
Review Days
101

Basic Information

Device Name
ZAVATION IBF SYSTEMS
K Number
K112664
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zavation, LLC
Date Received
September 13, 2011
Decision Date
December 23, 2011
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 Zavation, LLC

K Number Device Name
K162206 Zavation IBF
K162575 Z-LINKPC System
K162824 Z-Span Plate System
K161016 Z-Clamp ISP System
K153404 Zavation Spinal System
K160362 Z-Span Plate System
K142392 Zavation Posterior LEIF
K142271 Zavation Z-Link Lumbar
K141419 ZVPLASTY
K141005 Z-LINK CERVICAL
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