Clearance Summary
VIPER PRIME additions to the VIPER® System received FDA 510(k) clearance under submission number K162912, sponsored by Medos International SARL. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2016-12-08.
- Submission: K162912
- Applicant / Sponsor: Medos International SARL
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3070
- Decision date: 2016-12-08
Classification & Regulation
This clearance is catalogued under FDA product code NKB and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.