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

Z-Span Plate System

K Number: K160362 · Decision Mar 22, 2016
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
15
Review Days
42

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Basic Information

Device Name
Z-Span Plate System
K Number
K160362
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zavation, LLC
Date Received
February 9, 2016
Decision Date
March 22, 2016
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

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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
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 →