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

Atlas Spine Lateral Expandable Interbody System

K Number: K243191 · Decision Nov 26, 2024
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
15
Review Days
57

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Basic Information

Device Name
Atlas Spine Lateral Expandable Interbody System
K Number
K243191
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 30, 2024
Decision Date
November 26, 2024
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 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
K202302 Atlas Spine Rebar (Ti) Spacer System
K192570 Atlas Spine Expandable Cervical Standalone Interbody 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. →