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

Altus Spine Interbody Standalone Fusion System

K Number: K211837 · Decision Apr 19, 2022
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
17
Review Days
309

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Basic Information

Device Name
Altus Spine Interbody Standalone Fusion System
K Number
K211837
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
June 14, 2021
Decision Date
April 19, 2022
Product Code
OVD
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
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

Similar 510(k) Clearances

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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
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
K170553 Altus Spine Interbody Fusion System
Search all 17 clearances from Altus Partners, LLC →