Clearance Summary
AESCULAP BONE MILL received FDA 510(k) clearance under submission number K860016, sponsored by Aesculap Instruments Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1986-03-19.
- Submission: K860016
- Applicant / Sponsor: Aesculap Instruments Corp.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.4540
- Decision date: 1986-03-19
Classification & Regulation
This clearance is catalogued under FDA product code LYS and 21 CFR 888.4540, within the Orthopedic review panel as a Class I device.