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

Atlas Spine Expandable Cervical Interbody System

K Number: K180675 · Decision Jun 13, 2018
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
15
Review Days
90

Basic Information

Device Name
Atlas Spine Expandable Cervical Interbody System
K Number
K180675
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Atlas Spine, Inc.
Date Received
March 15, 2018
Decision Date
June 13, 2018
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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K Number Device Name
K252560 Atlas Spine HiRISE™ Expandable Cervical Corpectomy System
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K243191 Atlas Spine Lateral Expandable Interbody System
K202302 Atlas Spine Rebar (Ti) Spacer System
K192570 Atlas Spine Expandable Cervical Standalone Interbody System
K182418 V3 Segmental Plating 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
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