510(k) K860016
K860016 is an FDA 510(k) premarket notification submitted by Aesculap Instruments Corp. for the device "AESCULAP BONE MILL". The FDA issued a decision of Substantially Equivalent on March 19, 1986. The device falls under product code LYS (Bone Mill), a Class I device regulated under 21 CFR 888.4540. Aesculap Instruments Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 19, 1986
- Date Received
- January 3, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Bone Mill
- Device Class
- Class I
- Regulation Number
- 888.4540
- Review Panel
- OR
- Submission Type