Clearance Summary
LAKI HAND FIXATION SYSTEM, MODEL TFX.3X.06.X received FDA 510(k) clearance under submission number K082679, sponsored by Sintea Biotech, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2009-04-07.
- Submission: K082679
- Applicant / Sponsor: Sintea Biotech, Inc.
- Clearance pathway: Special
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 2009-04-07
Classification & Regulation
This clearance is catalogued under FDA product code JEC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.