7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
ILLUMINATOR II
FDA 510(k)
FDA Class 1
·General Hospital
OSTEOMED CRANIAL FLAP FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
OXFORD FIXED LATERAL BEARING PARTIAL KNEE REPLACEMENT (OXFORD TIBIAL TRAYS A-F) IXFORD PARTIAL KNEE REPLACEMENT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
T-PAL SPACER APPLICATOR INNER SHAFT
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code MAX·February 18, 2020
CAPSURE SP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010
TOTAL HIP BALL 32MM +11
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JDI·January 18, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HLTHACARE CORP·Product code FRN·February 5, 2014