7 results
·
17ms
·
Sources: EU EUDAMED, US FDA
HARPOON SUTURE ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
Arthrex®
FDA UDI
ARTHREX, INC.·00888867138407·DARRACH ELEVTR,14" LGX 1" WD,BLNT W/SERR
PRIME PCA AND PCA/CONTINUOUS SYSTEMS
FDA 510(k)
FDA Class 2
·General Hospital
OSTEO COMPRESSION HIP SCREW
FDA 510(k)
FDA Class 2
·Ophthalmic
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 17, 2014
SCREW LOCKING
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code HWC·January 23, 2013
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·November 10, 2010