Clearance Summary
INTERPORE CROSS CEMENT RESTRICTOR received FDA 510(k) clearance under submission number K032095, sponsored by Interpore Cross Intl.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2003-08-08.
- Submission: K032095
- Applicant / Sponsor: Interpore Cross Intl.
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.3300
- Decision date: 2003-08-08
Classification & Regulation
This clearance is catalogued under FDA product code JDK and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.