10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Momentum® Posterior Spinal Fixation System with G21 V-STEADY Bone Cement; Momentum® MIS Posterior Spinal Fixation System with G21 V-STEADY Bone Cement
FDA 510(k)
FDA Class 2
·Orthopedic
MILAGRO
FDA UDI
Medos International Sàrl·10886705010769·MILAGRO INTERFERENCE SCREW Absorbable - TCP/PLG...
PERIO PROTECT TRAY
FDA 510(k)
FDA Class 1
·Dental
AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DEPUY MITEK MILAGRO INTERFERENCE SCREW MODEL 231803, 231804, 231807, 231809
FDA 510(k)
FDA Class 2
·Orthopedic
6MM X 30MM MILAGRO SCREW
FDA Adverse Event
Injury
·DEPUY MITEK·Product code MAI·September 28, 2017
HEARTSTART XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·October 15, 2014
VANGUARD PS OPEN BOX FEMORAL 75MM RIGHT INTERLOK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·September 1, 2011
GYNECARE PROLIFT TOTAL PELVIC FLOOR REPAIR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·July 17, 2013
MILAGRO INSCR SMALL SIZE 6X30
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·August 3, 2021