Clearance Summary
SRM-STITCH 8F SRM-STITCH 8F WITH GUIDEWIRE received FDA 510(k) clearance under submission number K113763, sponsored by Nobles Medical Technologies Ii, Inc.. 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 2012-03-16.
- Submission: K113763
- Applicant / Sponsor: Nobles Medical Technologies Ii, Inc.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.5010
- Decision date: 2012-03-16
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.