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

Certex Spinal Fixation System

K Number: K160428 · Decision May 5, 2016
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
117
Applicant Total
34
Review Days
79

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Basic Information

Device Name
Certex Spinal Fixation System
K Number
K160428
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3075
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
X-Spine Systems, Inc.
Date Received
February 16, 2016
Decision Date
May 5, 2016
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.

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Other Clearances by X-Spine Systems, Inc.

K Number Device Name
K173832 InTice™-C Porous Ti Cervical Interbody System
K180153 X-spine Cortical Bone Screw System
K170119 Calix Lumbar Spinal Implant System
K171567 IRIX-A Lumbar Integrated Fusion System
K171075 Calix-C Cervical Interbody Spacer
K170224 Spider Cervical Plating System
K170530 Butrex Lumbar Buttress Plating System
K160959 Xsert Lumbar Expandable Interbody System
K162944 Irix-C Cervical Integrated Fusion System
K160114 Xspan Laminoplasty Fixation System
Search all 34 clearances from X-Spine Systems, Inc. →