Clearance Summary
SPIDER SYSTEM KOLIBRI CEMENT NEEDLE received FDA 510(k) clearance under submission number K130402, sponsored by Sintea Plustek, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2013-04-01.
- Submission: K130402
- Applicant / Sponsor: Sintea Plustek, LLC
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3027
- Decision date: 2013-04-01
Classification & Regulation
This clearance is catalogued under FDA product code NDN and 21 CFR 888.3027, within the Orthopedic review panel as a Class II device.