Clearance Summary
AESCULAP BONE WAX received FDA 510(k) clearance under submission number K000021, sponsored by Aesculap, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Unknown review panel. The statutory decision date of record is 2000-03-24.
- Submission: K000021
- Applicant / Sponsor: Aesculap, Inc.
- Clearance pathway: Traditional
- Review panel: Unknown
- Device class:
- Decision date: 2000-03-24
Classification & Regulation
This clearance is catalogued under FDA product code MTJ , within the Unknown review panel as a device.