9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
MOTOR DRIVE, MECHANICAL SECTOR SCANNING-MOD417
FDA 510(k)
FDA Class 2
·Cardiovascular
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690117537·Distal Reamer (Hudson)
ANGLED AUXILIARY CLAMP, LEFT
FDA UDI
MIZUHO ORTHOPEDIC SYSTEMS, INC.·00842430114618·
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690192602·Distal Reamer (Hudson)
GC85A
FDA 510(k)
FDA Class 2
·Radiology
MODIFICATION TO IFL PROFESSIONAL SYSTEM, MODEL C100
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TOTAL ASR FEM IMP SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·June 4, 2014
ELIMINATOR ICW
FDA Adverse Event
Malfunction
·ARTHROCARE CORPORATION·Product code GEI·November 21, 2012
PUMP MMT-522NAS PRDGM INS V2.2 SK EN
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·September 22, 2010