Medical Device Manufacturer · US , Fullerton , CA

Micomed GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1999

Recent clearances: MICOMED POSTERIOR DOUBLEROD SYSTEM (MPDS), MICOMED - HALM ZIELKE INSTRUMENTATION

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Micomed GmbH Orthopedic ✕

2 devices

1-2 of 2

Cleared Jan 13, 2000

MICOMED POSTERIOR DOUBLEROD SYSTEM (MPDS)

Orthopedic · 226d

Cleared Jan 20, 1999

MICOMED - HALM ZIELKE INSTRUMENTATION

Orthopedic · 226d