8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
MRL PACETTE, 450SLL
FDA 510(k)
FDA Class 2
·Cardiovascular
ELEVATE™ Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169430860·SPACER 8880932 ELEVATE X-LOR 32X9MM
Diamond Orthopedic Bone Fixation Screws and Pins
FDA 510(k)
FDA Class 2
·Orthopedic
MOSAIC LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TRULIANT TIB IMP PS INSERT SZ 4.5 13MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·April 26, 2024
INFINITI VISION SYSTEM OZIL
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·April 7, 2014
UNKNOWN DEPUY ASR ACETABULAR CUP
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code JDI·December 20, 2012
PARADYM
FDA Adverse Event
Malfunction
·SORIN BIOMEDICA CRM S.R.L.·Product code MRM·October 1, 2010