FasTouch™ Absorbable SFTA25
FasTouch™ Absorbable SFTA25 is a Class II device made by Via Surgical, Ltd., cleared under FDA 510(k) K181668 on 13 Mar 2019 and listed in FDA GUDID since 14 Sep 2019 (UDI-DI 07290017155241), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07290017155241 | Date14 Sep 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK181668 | Date13 Mar 2019 | StatusActive |
Official records
- AccessGUDID record 07290017155241
- FDA 510(k) database K181668
Across registries
- FDA 510(k) K181668 decided 13 Mar 2019 Active
- FDA GUDID UDI-DI 07290017155241 listed 14 Sep 2019 Listed
Timeline
- Cleared FDA 510(k) K181668
- Listed FDA GUDID 07290017155241
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- FasTouch™ Absorbable
- Generic name
- Soft-tissue/mesh anchor, bioabsorbable
- Model / Ref / Catalog
- SFTA25
- Primary DI / UDI-DI
- 07290017155241
- 510(k) Number
- FDA product code
- GDW
- GMDN term
- Soft-tissue/mesh anchor, bioabsorbable
- Device class
- Class II
- Regulation number
- 878.4750
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
- Size
- Outer Diameter — 5 MillimeterLength — 37 Centimeter
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