Clearance Summary
Modulift Vertebral Body Replacement (VBR) System received FDA 510(k) clearance under submission number K172032, sponsored by Aesculap Implants Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2017-11-20.
- Submission: K172032
- Applicant / Sponsor: Aesculap Implants Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3060
- Decision date: 2017-11-20
Classification & Regulation
This clearance is catalogued under FDA product code PLR and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.