6 results
·
42ms
·
Sources: EU EUDAMED, US FDA
KNEE INSTRUMENTATION, CONDYLAR
FDA 510(k)
FDA Class 1
·Orthopedic
AxSOS 3 Ti
FDA 510(k)
FDA Class 2
·Orthopedic
PRECISION 500D R&F X-RAY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
LIGAMAX 5MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·April 30, 2014
VITALITY 2
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 10, 2012
SWARTZ BRAIDED TRANS. GUIDING INT., 8F, SLO
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, AF DIV·Product code DYB·July 29, 2010