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Manufacturers
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Stork Instrumente GmbH
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Medical Device Manufacturer
·
US , Gurnee , IL
Stork Instrumente GmbH - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2003
Recent clearances:
BONE WIRE
View 1 510(k) Devices ↓
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Stork Instrumente GmbH
Orthopedic
✕
1
devices
1-1 of 1
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Cleared
Mar 25, 2003
BONE WIRE
K030665
·
HTY
Orthopedic
·
22d
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