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

Atlas Spine Expandable Cervical Standalone Interbody System

K Number: K192570 · Decision Feb 28, 2020
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
161
Applicant Total
15
Review Days
163

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Basic Information

Device Name
Atlas Spine Expandable Cervical Standalone Interbody System
K Number
K192570
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Atlas Spine, Inc.
Date Received
September 18, 2019
Decision Date
February 28, 2020
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

Other 510(k) clearances with the same product code (OVE), ordered by most recent decision date.

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Other Clearances by Atlas Spine, Inc.

K Number Device Name
K252560 Atlas Spine HiRISE™ Expandable Cervical Corpectomy System
K251969 Atlas Spine Project X Expandable Posterior Lumbar Interbody System
K243191 Atlas Spine Lateral Expandable Interbody System
K202302 Atlas Spine Rebar (Ti) Spacer System
K182418 V3 Segmental Plating System
K180675 Atlas Spine Expandable Cervical Interbody System
K172334 Ortus™ Expandable Lumbar Interbody Fusion System
K162918 Atlas Spine Expandable Interbody System
K112759 APCLO PEDICLE SCREW SYSTEMS
K110842 ATLAS SPINE PEDICLE SCREW SYSTEM
Search all 15 clearances from Atlas Spine, Inc. →