Clearance Summary
ACTIFUSE FLOW BONE GRAFT SUBSTITUTE received FDA 510(k) clearance under submission number K082073, sponsored by Apatech , 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 2008-09-11.
- Submission: K082073
- Applicant / Sponsor: Apatech , Ltd.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3045
- Decision date: 2008-09-11
Classification & Regulation
This clearance is catalogued under FDA product code MQV and 21 CFR 888.3045, within the Orthopedic review panel as a Class II device.