Device Classification Name |
shoulder prosthesis, reverse configuration
|
510(k) Number |
K191960 |
Device Name |
Arthrex Univers Revers Modular Glenoid System |
Applicant |
Arthrex Inc. |
1370 Creekside Boulevard |
Naples,
FL
34108 -1945
|
|
Applicant Contact |
Ivette Galmez |
Correspondent |
Arthrex Inc. |
1370 Creekside Boulevard |
Naples,
FL
34108 -1945
|
|
Correspondent Contact |
Ivette Galmez |
Regulation Number | 888.3660
|
Classification Product Code |
|
Date Received | 07/23/2019 |
Decision Date | 12/23/2019 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Orthopedic
|
510k Review Panel |
Orthopedic
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|