Clearance Summary
ReliaTack Articulating Reloadable Fixation Device with Deep Purchase Reloadable Tacks received FDA 510(k) clearance under submission number K151659, sponsored by Covidien, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2015-07-17.
- Submission: K151659
- Applicant / Sponsor: Covidien, LLC
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4750
- Decision date: 2015-07-17
Classification & Regulation
This clearance is catalogued under FDA product code GDW and 21 CFR 878.4750, within the General, Plastic Surgery review panel as a Class II device.