Co-Ligne AG

Co-Ligne AG holds 4 FDA 510(k) medical device clearances, first cleared 2004, most recent 2009.

Top product codes for Co-Ligne AG

MNH — Orthopedic3 devices
MQP — Orthopedic1 device

Recent clearances by Co-Ligne AG

K083567 — GII SPINAL FIXATION SYSTEM, GII-TI-POLY AXIAL SCREWCode MNH·2009-09-14
K072326 — OSTAPEK VBR SYSTEMCode MQP·2008-06-24
K051089 — GII SPINAL FIXATION SYSTEMCode MNH·2005-10-26
K032604 — GII SPINAL FIXATION SYSTEMCode MNH·2004-01-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.