Clearance Summary
MODIFICATION TO TRELEX MESH SURGICAL MESH received FDA 510(k) clearance under submission number K020110, sponsored by Boston Scientific. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2002-04-03.
- Submission: K020110
- Applicant / Sponsor: Boston Scientific
- Clearance pathway: Abbreviated
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.3300
- Decision date: 2002-04-03
Classification & Regulation
This clearance is catalogued under FDA product code OTN and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.