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

CALIX PC SPINAL IMPLANT SYSTEM

K Number: K112036 · Decision Nov 8, 2011
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
34
Review Days
113

Basic Information

Device Name
CALIX PC SPINAL IMPLANT SYSTEM
K Number
K112036
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
July 18, 2011
Decision Date
November 8, 2011
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

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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. →