510(k) K221936

Device
Standalone ALIF Interbody Fusion System
Applicant
Eminent Spine
510(k) number
K221936
Product code
OVD
Decision
Substantially Equivalent (SESE)
Decision date
2022-10-17
Date received
2022-07-01
Regulation
888.3080
Classification name
Intervertebral Fusion Device With Integrated Fixation, Lumbar
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Stephen Courtney
Address
2004 Ventura Dr. Suite 100 Plano TX US 75093 75093

FDA Registration Numbers

Source Documents

510(k) summary PDF

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