Clearance Summary
NEOTIS; NEOTIS 50 received FDA 510(k) clearance under submission number K130953, sponsored by Sbm Sciences For Bio Materials. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2013-07-15.
- Submission: K130953
- Applicant / Sponsor: Sbm Sciences For Bio Materials
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3045
- Decision date: 2013-07-15
Classification & Regulation
This clearance is catalogued under FDA product code MQV and 21 CFR 888.3045, within the Orthopedic review panel as a Class II device.