510(k) K223153

Device
Catalyft LS Expandable Interbody System with Titan nanoLOCK Surface Technology
Applicant
Medtronic Sofamor Danek USA, Inc.
510(k) number
K223153
Product code
MAX
Decision
Substantially Equivalent (SESE)
Decision date
2022-12-16
Date received
2022-10-06
Regulation
888.3080
Classification name
Intervertebral Fusion Device With Bone Graft, Lumbar
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Alex Underberg
Address
1800 Pyramid Pl. Memphis TN US 38132 38132

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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