Medical Device Manufacturer · US , Lake Forest , CA

Micomed Ortho GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Recent clearances: HALM ZIELKE INSTRUMENTATION SYSTEM, MICOMED POSTERIOR DOUBLEROD SYSTEM

View 2 510(k) Devices ↓
2
Total
2
Cleared
0
Denied

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

2 devices
1-2 of 2
Cleared Sep 22, 2003
HALM ZIELKE INSTRUMENTATION SYSTEM
K024125 · KWQ
Orthopedic · 280d
Cleared Jul 18, 2002
MICOMED POSTERIOR DOUBLEROD SYSTEM
K021275 · MNI
Orthopedic · 87d
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