Clearance Summary
EOS SPINAL SYSTEM received FDA 510(k) clearance under submission number K082509, sponsored by Korea Bone Bank Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2008-12-15.
- Submission: K082509
- Applicant / Sponsor: Korea Bone Bank Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3070
- Decision date: 2008-12-15
Classification & Regulation
This clearance is catalogued under FDA product code MNH and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.