Clearance Summary
Triton Sponge System received FDA 510(k) clearance under submission number K163507, sponsored by Gauss Surgical, Inc.,. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2017-04-25.
- Submission: K163507
- Applicant / Sponsor: Gauss Surgical, Inc.,
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.2750
- Decision date: 2017-04-25
Classification & Regulation
This clearance is catalogued under FDA product code PBZ and 21 CFR 880.2750, within the General Hospital review panel as a Class II device.