Stork Instrumente GmbH

Stork Instrumente GmbH holds 1 FDA 510(k) medical device clearance, cleared in 2003.

Top product codes for Stork Instrumente GmbH

HTY — Orthopedic1 device

Recent clearances by Stork Instrumente GmbH

K030665 — BONE WIRECode HTY·2003-03-25

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