11 results
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18ms
·
Sources: EU EUDAMED, US FDA
TRACET AG 4000
FDA 510(k)
FDA Class 2
·Cardiovascular
ReLine
FDA UDI
Nuvasive, Inc.·00195377068972·RELINE C Screw, 4.5x12mm MA
VuePoint
FDA UDI
Nuvasive, Inc.·00887517178909·VuePoint Screw, 5x12mm Cort Occipital
NP UCLA Abutment Plastic, Non-Hexed
FDA UDI
STERNGOLD DENTAL LLC·00841549111747·The UCLA-Type Abutment is attached directly to ...
Solstice Occipito-Cervico-Thoracic System
FDA UDI
Life Spine, Inc.·00190837014681·
Duo Lumbar Interbody Fusion Device
FDA UDI
SPINEOLOGY INC.·M7402904512·Duo, Non-Lordotic, 45 x 12mm
SIEMENS ELEMA MODELS 4020T AND 4021T ADAPTERS
FDA 510(k)
FDA Class 2
·Cardiovascular
L SOPHIA
FDA 510(k)
FDA Unclassified
·Unknown
3002 SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·November 30, 2012
INTEGRATED APD SET W/CASSETTE3 PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·November 22, 2010
TELIGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014