Rotec Medizintechnik GmbH

Rotec Medizintechnik GmbH holds 2 FDA 510(k) medical device clearances, cleared in 2000.

Top product codes for Rotec Medizintechnik GmbH

LZO — Orthopedic2 devices

Recent clearances by Rotec Medizintechnik GmbH

K992359 — MRS-TITANCode LZO·2000-02-18
K992403 — MRP-TITANCode LZO·2000-01-21

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