Medical Device Manufacturer · US , Kalamazoo , MI

Stryker Leibinger - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1999
12
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - Stryker Leibinger Orthopedic ✕
2 devices
1-2 of 2
Cleared Mar 12, 2004
STRYKER LEIBINGER UNIVERSAL DISTAL RADIUS SYSTEM
K040022 · HRS
Orthopedic · 65d
Cleared Jan 08, 2002
TWINFIX INTERFRAGMENTARY COMPRESSION SCREW SYSTEM
K013775 · HRS
Orthopedic · 56d
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All12 General & Plastic Surgery 3 Neurology 3 Radiology 2 Orthopedic 2 Dental 2