Clearance Summary
ZYSTON ARC INTERBODY SPACER received FDA 510(k) clearance under submission number K110650, sponsored by Biomet Spine (Aka Ebi, LLC). The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-06-30.
- Submission: K110650
- Applicant / Sponsor: Biomet Spine (Aka Ebi, LLC)
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3080
- Decision date: 2011-06-30
Classification & Regulation
This clearance is catalogued under FDA product code MAX and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.