The following data is part of a premarket notification filed by Caldera Medical, Inc. with the FDA for Desara Mesh, Desara Blue.
| Device ID | K132069 |
| 510k Number | K132069 |
| Device Name: | DESARA MESH, DESARA BLUE |
| Classification | Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator |
| Applicant | CALDERA MEDICAL, INC. 5171 CLARETON DRIVE Agoura Hills, CA 91301 |
| Contact | Vicki Gail |
| Correspondent | Vicki Gail CALDERA MEDICAL, INC. 5171 CLARETON DRIVE Agoura Hills, CA 91301 |
| Product Code | OTN |
| CFR Regulation Number | 878.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-07-03 |
| Decision Date | 2013-09-23 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00890594000674 | K132069 | 000 |
| 00890594000889 | K132069 | 000 |