7 results
·
27ms
·
Sources: EU EUDAMED, US FDA
ROTATION AIR FLUIDIZED BED/DELTA
FDA 510(k)
FDA Class 2
·Physical Medicine
PHARMASEAL SCRUB CARE-SURGICAL SCRUB BRUSH SPONGES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
VAS-CATH DSA CATHETER/TRAY
FDA 510(k)
FDA Class 2
·Cardiovascular
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 10, 2014
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·October 11, 2010
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·December 10, 2012
OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·October 13, 2021