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

Altus Spine Cervical Interbody Fusion System

K Number: K172253 · Decision Nov 21, 2017
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
17
Review Days
118

Basic Information

Device Name
Altus Spine Cervical Interbody Fusion System
K Number
K172253
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Altus Partners, LLC
Date Received
July 26, 2017
Decision Date
November 21, 2017
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 Altus Partners, LLC

K Number Device Name
K243419 Altus Spine Navigation System
K211027 Altus Spine Pedicle Screw System
K211837 Altus Spine Interbody Standalone Fusion System
K210887 Altus Spine Sochi OCT Spinal System
K200922 Altus Spine HA Pedicle Screw System
K200322 Altus Spine Pedicle Screw System
K183084 Fuji Cervical Plate System
K182406 Altus Spine Interbody Fusion System
K181339 Altus Spine Pedicle Screw System
K181281 Altus Spine Pedicle Screw System
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