10 results
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16ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Completed
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IceRod" 1.5 MRI Cryoablation Needle
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
IceSeed" 1.5 MRI Cryoablation Needle
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
IceSeed" 1.5 MRI 90 Cryoablation Needle
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
IceRod" 1.5 MRI 90 Cryoablation Needle
FDA Recall
Completed
·Boston Scientific Corporation·Product code GEH·November 18, 2020
IceSeed" 1.5 MRI Cryoablation Needle
FDA Enforcement
Class II
·Completed·Boston Scientific Corporation·December 30, 2020
IceRod" 1.5 MRI Cryoablation Needle¿
FDA Enforcement
Class II
·Completed·Boston Scientific Corporation·December 30, 2020
IceSeed" 1.5¿ MRI 90¿ Cryoablation Needle ¿
FDA Enforcement
Class II
·Completed·Boston Scientific Corporation·December 30, 2020
IceRod" 1.5 MRI 90¿ Cryoablation Needle¿
FDA Enforcement
Class II
·Completed·Boston Scientific Corporation·December 30, 2020
MRI Biomet Pin Guide for Total Knee Arthroplasty (Zimmer Biomet Patient Specific Instruments (PSI)-- patient-matched device designed to fit the patients anatomy to transfer a patient-specific pre-operative plan to the OR. Ref: KNM-ZB02-00-01
FDA Enforcement
Class II
·Completed·Materialise N.V.·July 26, 2023
MRI Biomet Pin Guide for Total Knee Arthroplasty (Zimmer Biomet Patient Specific Instruments (PSI)-- patient-matched device designed to fit the patients anatomy to transfer a patient-specific pre-operative plan to the OR. Ref: KNM-ZB02-00-01
FDA Recall
Completed
·Materialise N.V. Technologielaan 15 Heverlee Belgium·Product code JWH·April 26, 2023