Clearance Summary
LANCER PEDICLE SCREW SYSTEM received FDA 510(k) clearance under submission number K110633, sponsored by Spinal Solutions, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-12-15.
- Submission: K110633
- Applicant / Sponsor: Spinal Solutions, LLC
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3070
- Decision date: 2011-12-15
Classification & Regulation
This clearance is catalogued under FDA product code MNH and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.