6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KLIMT Expandable Lumbar Interbody Fusion (LIF) Cage System
FDA 510(k)
FDA Class 2
·Orthopedic
IRIX-A LUMBAR INTEGRATED FUSION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SHIRAZ POSTERIOR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
EEA 25MM STAPLER WITH 3.5MM STAPLES
FDA Adverse Event
Injury
·NORTH HAVEN - USS·Product code GDW·November 14, 2008
ACIST
FDA Adverse Event
Injury
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·August 30, 2011
REMB MICRO DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code HBE·July 18, 2013