Stuckenbrock Medizintechnik GmbH

Stuckenbrock Medizintechnik GmbH holds 3 FDA 510(k) medical device clearances, first cleared 2004, most recent 2018.

Top product codes for Stuckenbrock Medizintechnik GmbH

Recent clearances by Stuckenbrock Medizintechnik GmbH

K171624 — IXOS Radius Plate SystemCode HRS·2018-03-29
K171628 — HBS2 Headless Bone ScrewCode HWC·2018-01-12
K042902 — HERBERT ULNAR HEAD PROSTHESIS SYSTEMCode KXE·2004-12-27

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