Ackermann Instrumente GmbH

Ackermann Instrumente GmbH holds 3 FDA 510(k) medical device clearances, first cleared 1998, most recent 2015.

Top product codes for Ackermann Instrumente GmbH

Recent clearances by Ackermann Instrumente GmbH

K143450 — Ackermann Intervertebral Body Fusion DeviceCode ODP·2015-09-16
K111930 — ACKERMANN EUROPCLIPCode FZP·2011-11-08
K974382 — ACKERMANN SURGICAL INSTRUMENTSCode GCJ·1998-04-21

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