Device Classification Name |
intervertebral fusion device with bone graft, lumbar
|
510(k) Number |
K191796 |
Device Name |
Neo Cage System |
Applicant |
Neo Medical S.A. |
Route de Lausanne 157A |
Villette (Lavaux),
CH
1096
|
|
Applicant Contact |
Jonas Larsson |
Correspondent |
Confinis Corporation |
15807 Glacier Ct |
North Potomac,
MD
20878
|
|
Correspondent Contact |
Charles Cathlin |
Regulation Number | 888.3080
|
Classification Product Code |
|
Date Received | 07/03/2019 |
Decision Date | 12/13/2019 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|