8 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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7000 SERIES TOTAL KNEE PATELLAR COMPONENTS
FDA 510(k)
FDA Class 2
·Orthopedic
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471123175·K-WIRE - SINGLE TROCAR THREADED 1.8mm DIA x 150mm
WYMAN SUTURE WASHER
FDA 510(k)
FDA Class 2
·Orthopedic
GERI TOTAL HIP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CONSTRAINED LINER WITH CONSTRAINING RING 36 MM
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code KWZ·August 27, 2020
S-ICD SYSTEM
FDA Adverse Event
Malfunction
·CAMERON HEALTH·Product code NVY·May 16, 2014
DEPUY ASR XL FEM IMP SIZE 55
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·January 15, 2013
DA VINCI SI SURGICAL SYSTEM
FDA Adverse Event
Other
·INTUITIVE SURGICAL,INC.·Product code NAY·December 6, 2010