6 results
·
35ms
·
Sources: EU EUDAMED, US FDA
BREEZE DIGITAL INFLATION DEVICE
FDA 510(k)
FDA Class 2
·Cardiovascular
CORUS Posterior Cervical Stabilization System 3D (CORUS PCSS 3D)
FDA 510(k)
FDA Unclassified
·Unknown
OSTEON III
FDA 510(k)
FDA Class 2
·Dental
VIRTUOSO DR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 9, 2013
CONTAK RENEWAL
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 10, 2011
BIOMET GRIT BLASTED KNEE STEM 16X80
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·July 23, 2014