Clearance Summary
GMD UNIVERSAL SLING, MODEL PRODUCT CODE 1010 AND 1020 received FDA 510(k) clearance under submission number K083471, sponsored by Generic Medical Device, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2009-03-03.
- Submission: K083471
- Applicant / Sponsor: Generic Medical Device, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.3300
- Decision date: 2009-03-03
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.