FasTouch Absorbable Fixation System
510(k) K181668
FasTouch Absorbable Fixation System is a Class II device made by Via Surgical, Ltd., cleared under FDA 510(k) K181668 on 13 Mar 2019, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK181668 | Date13 Mar 2019 | StatusActive |
Official records
- FDA 510(k) database K181668
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- GDW
- FDA applicant
- Via Surgical , Ltd.
- Device class
- Class II
- Regulation
- 21 CFR Part 878.4750
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K181668
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| FasTouch™ Absorbable FTA25 | FTA25 / FTA25 | 07290017155210 | Outer Diameter 5 mm; Length 37 cm | On the market |
| FasTouch™ Absorbable FTAC10 | FTAC10 / FTAC10 | 07290017155272 | Outer Diameter 5 mm; Length 37 cm | On the market |
| FasTouch™ Absorbable SFTA25 | SFTA25 / SFTA25 | 07290017155241 | Outer Diameter 5 mm; Length 37 cm | On the market |
| FasTouch™ Absorbable SFTAC10 | SFTAC10 / SFTAC10 | 07290017155289 | Outer Diameter 5 mm; Length 37 cm | On the market |
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