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

IRIX-C CERVICAL INTEGRATED FUSION SYSTEM

K Number: K131951 · Decision Aug 14, 2013
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
161
Applicant Total
34
Review Days
48

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Basic Information

Device Name
IRIX-C CERVICAL INTEGRATED FUSION SYSTEM
K Number
K131951
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
X-Spine Systems, Inc.
Date Received
June 27, 2013
Decision Date
August 14, 2013
Product Code
OVE
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
OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

Similar 510(k) Clearances

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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
K160428 Certex Spinal Fixation System
Search all 34 clearances from X-Spine Systems, Inc. →