Clearance Summary
PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE received FDA 510(k) clearance under submission number K990131, sponsored by Interpore Cross Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1999-03-02.
- Submission: K990131
- Applicant / Sponsor: Interpore Cross Intl.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3045
- Decision date: 1999-03-02
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.