Clearance Summary
RECON system- Grubber Lapidus-, Platar Lapidus-, Tarsalis Plates and Screws received FDA 510(k) clearance under submission number K152256, sponsored by Normed Medizin-Technik GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2015-11-05.
- Submission: K152256
- Applicant / Sponsor: Normed Medizin-Technik GmbH
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3030
- Decision date: 2015-11-05
Classification & Regulation
This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.