7 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
FMS DUO
FDA 510(k)
FDA Class 2
·Orthopedic
LINK CONTOUR RIBBED HIP PROSTHESES SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
FLEXIBLE ARTHROSCOPE
FDA 510(k)
FDA Class 2
·Orthopedic
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·July 1, 2011
CAPSURE SP
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·February 11, 2013
ASR ACETABULAR CUPS 56
FDA Adverse Event
Injury
·DEPUY INTL., LTD.·Product code KWA·January 5, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·July 24, 2014