Clearance Summary
HERNIASTAT received FDA 510(k) clearance under submission number K884404, sponsored by Innovative Surgical Devices Corp.. 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 1988-11-08.
- Submission: K884404
- Applicant / Sponsor: Innovative Surgical Devices Corp.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 878.4740
- Decision date: 1988-11-08
Classification & Regulation
This clearance is catalogued under FDA product code GAG and 21 CFR 878.4740, within the General Hospital review panel as a Class II device.