6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SPINAL NEEDLES
FDA 510(k)
FDA Class 2
·Anesthesiology
PIONEER VERTEBRAL SPACER (VERTEBRAL SPACER)
FDA 510(k)
FDA Class 2
·Orthopedic
Spinal fixation system
FDA 510(k)
FDA Class 2
·Orthopedic
INRATIO2
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·February 8, 2013
ESSURE
FDA Adverse Event
Injury
·BAYER·Product code HHS·July 23, 2014
FLEXICAP DISCONNECT CAP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·January 14, 2011