AMS SACRAL COLPOPEXY SLING, MODEL 72403501
FDA 510(k) clearance K010931 · decided 2001-04-09
Clearance details
- K-number
- K010931
- Device name
- AMS SACRAL COLPOPEXY SLING, MODEL 72403501
- Applicant
- American Medical Systems, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2001-03-28
- Decision date
- 2001-04-09
- Days to decision
- 12 days
- Clearance type
- Special
- Product code
- OTO
- Device class
- 2
- Regulation number
- 878.3300
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Minnetonka, MN, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch American Medical Systems
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| Polyform Synthetic Mesh (K171271) | Boston Scientific Corporation | 2017-12-15 |
| Vertessa Lite Y-Mesh (K150023) | Caldera Medical, Inc. | 2015-04-06 |
| Vertessa Lite (K150016) | Caldera Medical, Inc. | 2015-04-06 |
| RESTORELLE Y CONTOUR MESH (K140116) | Coloplast A/S | 2014-02-12 |
| RESTORELLE M, RESTORELLE XL (K132061) | Coloplast Corp. | 2013-08-02 |
| VERTESSA LITE 10 X20CM, VERTESSA LITE 11 X 30CM, VERTESSA LITE Y-MESH (K123028) | Caldera Medical, Inc. | 2013-04-25 |
| RESTORELLE Y CONTOUR (K123914) | Coloplast A/S | 2013-03-05 |
| VERTESSA LITE 10 X 20CM, VERTESSA LITE 11 X 30CM (K123337) | Caldera Medical | 2013-02-21 |
| UPSYLON Y MESH (K122794) | Boston Scientific Corp | 2012-12-18 |
| NOVASILK MESH QTY 1 MODEL 93-6014, NOVASILK MESH QTY 3 MODEL 93-6015 (K122968) | Coloplast Corp. | 2012-12-18 |
| RESTORELLE L (K122440) | Coloplast Corp. | 2012-11-19 |
| AMS LARGE PORE POLYPROPHLENE MESH (K121805) | American Medical Systems | 2012-10-16 |
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| 600 SERIES DYE MODULES (MODELS 630 AND 630 XP) AND SERIES 700 AND 800 KTP/532 AND KTP/YAG SURGICAL LASERS (P940012/S002) | American Medical Systems, Inc. | 1998-12-23 |
| 600 SERIES DYE MODULES (MODELS 630 AND 630 XP) AND SERIES 700 AND 800 KTP/532 AND KTP/YAG SURGICAL LASERS (P940012/S001) | American Medical Systems, Inc. | 1998-01-09 |
| 600 SERIES DYE MODULES (MODELS 630 AND 630 XP) AND SERIES 700 AND 800 KTP/532 AND KTP/YAG SURGICAL LASERS (P940012) | American Medical Systems, Inc. | 1995-12-27 |