8 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MODULAR ACETABULAR SHELL II
FDA 510(k)
FDA Class 2
·Orthopedic
#903 SILAFLEX II
FDA 510(k)
FDA Unclassified
·Unknown
ZIMMER CERAMIC FEMORAL HEADS
FDA 510(k)
FDA Class 2
·Orthopedic
PINNACLE MTL INS NEUT36IDX56OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·October 10, 2013
S-ROM M HEAD 36MM +0
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·October 10, 2013
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Injury
·ZOLL MANUFACTURING CORPORATION·Product code MVK·July 31, 2015
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 11, 2013
CPOE/EHR DEVICE
FDA Adverse Event
Injury
·PRO TOUCH/KINDRED·Product code NSX·July 21, 2014