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

SPINEOLOGY PEEK LUMBAR INTERBODY FUSION DEVICE

K Number: K110933 · Decision Jun 13, 2011
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
54
Review Days
70

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SPINEOLOGY PEEK LUMBAR INTERBODY FUSION DEVICE
K Number
K110933
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spineology, Inc.
Date Received
April 4, 2011
Decision Date
June 13, 2011
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Similar 510(k) Clearances

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

View all

Other Clearances by Spineology, Inc.

K Number Device Name
K251302 OptiMesh Multiplanar Expandable Interbody Fusion System
K251943 Spineology Navigation Instruments
K230927 OptiMesh Multiplanar Expandable Interbody Fusion System
K231781 OptiMesh Multiplanar Expandable Interbody Fusion System
K213876 Spineology Navigation Instruments
K210155 Duo Expandable Interbody Fusion System
DEN200010 Spineology Interbody Fusion System
K192047 Rampart™ One Lumbar Interbody Fusion System
K191091 Rampart One Lumbar Interbody Fusion System
K190055 Duo Lumbar Interbody Fusion Device
Search all 54 clearances from Spineology, Inc. →