Micomed GmbH

Micomed GmbH holds 2 FDA 510(k) medical device clearances, first cleared 1999, most recent 2000.

Top product codes for Micomed GmbH

KWQ — Orthopedic1 device
MNI — Orthopedic1 device

Recent clearances by Micomed GmbH

K991862 — MICOMED POSTERIOR DOUBLEROD SYSTEM (MPDS)Code MNI·2000-01-13
K982006 — MICOMED - HALM ZIELKE INSTRUMENTATIONCode KWQ·1999-01-20

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