Verticor, Ltd.

Verticor, Ltd. holds 3 FDA 510(k) medical device clearances, first cleared 2009, most recent 2011.

Top product codes for Verticor, Ltd.

Recent clearances by Verticor, Ltd.

K110047 — VERTICOR K-WIRE SYSTEMCode HTY·2011-02-28
K103137 — VENUS ANTERIOR CERVICAL PLATECode KWQ·2011-02-10
K091426 — CERVICORE CORPECTOMY CAGECode MQP·2009-12-23

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