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

Altus Spine Sochi OCT Spinal System

K Number: K210887 · Decision Aug 20, 2021
Classifications
1
FEI Numbers
164
Registration Numbers
164
Same Product Code
117
Applicant Total
17
Review Days
148

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Basic Information

Device Name
Altus Spine Sochi OCT Spinal System
K Number
K210887
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3075
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Altus Partners, LLC
Date Received
March 25, 2021
Decision Date
August 20, 2021
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 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
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 →