Wallflextm Biliary Rx Stent System (Uncovered, Partially Covered, and Fully Covered) Wallflextm Biliary Transhepatic Ste
510(k) K122072
Active
510(k)
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESU | NumberK122072 | Date28 Sep 2012 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- FGE
- FDA applicant
- Boston Scientific Corporation
- Device class
- Class II
- Regulation
- 21 CFR Part 876.5010
- Advisory committee
- Gastroenterology, Urology
- FDA decision
- SESU