Clearance Summary
ORTHOPILOT 2 TOTAL HIP ARTHROPLASTY (THA) VERSION 3.0 received FDA 510(k) clearance under submission number K072899, sponsored by Aesculap Implant Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2008-02-06.
- Submission: K072899
- Applicant / Sponsor: Aesculap Implant Systems, Inc.
- Clearance pathway: Special
- Review panel: Neurology
- Device class: Class II
- Regulation citation: 21 CFR 882.4560
- Decision date: 2008-02-06
Classification & Regulation
This clearance is catalogued under FDA product code HAW and 21 CFR 882.4560, within the Neurology review panel as a Class II device.