10 results
·
17ms
·
Sources: EU EUDAMED, US FDA
ORIGIN SECONDARY CANNULA AND TROCAR
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Clydesdale™ Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994972422·CAGE 2922460 CLYDESDALE 22 12DEG 14X60
CLYDESDALE PTC™ Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169191259·CAGE 4922460 CDALE PTC 22MM 12 DEG 14X60
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613089603·J-Shaped Electrode, Insulated, Overall Length 1...
LARGE AO COUPLING ASNIS III HALL FITTING
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·September 25, 2012
SMITH & NEPHEW IMAGE GUIDED SURGICAL SYSTEM FOR KNEE APPLICATIONS
FDA 510(k)
FDA Class 2
·Neurology
Intraoperative Ultrasound Probe Cover
FDA 510(k)
FDA Class 2
·Radiology
DUR MAR 10D LINER 28IDX58OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·January 18, 2013
CAPSUREFIX
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010
INRATIO PT/INR TEST STRIPS
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·June 2, 2014