Clearance Summary
AESCULAP ORTHOPILOT NEXT GENERATION received FDA 510(k) clearance under submission number K141694, sponsored by Aesculap Implant Systems, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2015-02-24.
- Submission: K141694
- Applicant / Sponsor: Aesculap Implant Systems, LLC
- Clearance pathway: Special
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4560
- Decision date: 2015-02-24
Classification & Regulation
This clearance is catalogued under FDA product code OLO and 21 CFR 882.4560, within the Neurology review panel as a Class II device.