Clearance Summary
ATLANTIK received FDA 510(k) clearance under submission number K070794, sponsored by Medical Biomat. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2007-07-10.
- Submission: K070794
- Applicant / Sponsor: Medical Biomat
- Clearance pathway: Abbreviated
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3045
- Decision date: 2007-07-10
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.