Device Classification Name |
intervertebral fusion device with bone graft, lumbar
|
510(k) Number |
K223153 |
Device Name |
Catalyft LS Expandable Interbody System with Titan nanoLOCK Surface Technology |
Applicant |
Medtronic Sofamor Danek USA, Inc. |
1800 Pyramid Place |
Memphis,
TN
38132
|
|
Applicant Contact |
Alex Underberg |
Correspondent |
Medtronic Sofamor Danek USA, Inc. |
1800 Pyramid Place |
Memphis,
TN
38132
|
|
Correspondent Contact |
Alex Underberg |
Regulation Number | 888.3080
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 10/06/2022 |
Decision Date | 12/16/2022 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|