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

ATLAS SPINE SPACER

K Number: K081880 · Decision Oct 2, 2008
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
15
Review Days
92

Basic Information

Device Name
ATLAS SPINE SPACER
K Number
K081880
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
July 2, 2008
Decision Date
October 2, 2008
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
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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
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