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

Z-LINKPC System

K Number: K162575 · Decision Mar 3, 2017
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
117
Applicant Total
15
Review Days
169

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Z-LINKPC System
K Number
K162575
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3075
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zavation, LLC
Date Received
September 15, 2016
Decision Date
March 3, 2017
Product Code
NKG
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
NKG Posterior Cervical Screw System

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NKG), ordered by most recent decision date.

View all

Other Clearances by Zavation, LLC

K Number Device Name
K162206 Zavation IBF
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 →