Device Classification Name |
mesh, surgical, synthetic, urogynecologic, for stress urinary incontinence, retropubic or transobturator
|
510(k) Number |
K132069 |
Device Name |
DESARA MESH, DESARA BLUE |
Applicant |
CALDERA MEDICAL, INC. |
5171 CLARETON DRIVE |
AGOURA HILLS,
CA
91301
|
|
Applicant Contact |
VICKI GAIL |
Correspondent |
CALDERA MEDICAL, INC. |
5171 CLARETON DRIVE |
AGOURA HILLS,
CA
91301
|
|
Correspondent Contact |
VICKI GAIL |
Regulation Number | 878.3300
|
Classification Product Code |
|
Date Received | 07/03/2013 |
Decision Date | 09/23/2013 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
Gastroenterology/Urology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|