Medical Device Manufacturer · US , Redwood City , CA

Laurimed, LLC - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2008
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Laurimed, LLC Orthopedic ✕
2 devices
1-2 of 2
Cleared May 21, 2009
PERCUTANEOUS DISCECTOMY SYSTEM
K090815 · HRX
Orthopedic · 57d
Cleared Aug 28, 2008
LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002
K082194 · HRX
Orthopedic · 24d
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