Clearance Summary
COPIOS BONE VOID FILLER SPONGE AND PASTE received FDA 510(k) clearance under submission number K071237, sponsored by Kensey Nash Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2007-06-01.
- Submission: K071237
- Applicant / Sponsor: Kensey Nash Corp.
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3045
- Decision date: 2007-06-01
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.