Clearance Summary
Deklene MAXX received FDA 510(k) clearance under submission number K193530, sponsored by Teleflex Medical. 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 2020-03-19.
- Submission: K193530
- Applicant / Sponsor: Teleflex Medical
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.5010
- Decision date: 2020-03-19
Classification & Regulation
This clearance is catalogued under FDA product code GAW and 21 CFR 878.5010, within the General, Plastic Surgery review panel as a Class II device.