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

Zavation IBF

K Number: K162206 · Decision Apr 4, 2017
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
15
Review Days
242

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Basic Information

Device Name
Zavation IBF
K Number
K162206
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
August 5, 2016
Decision Date
April 4, 2017
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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Other Clearances by Zavation, LLC

K Number Device Name
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
K130030 ZAVATION CERVICAL PLATE SYSTEM
Search all 15 clearances from Zavation, LLC →