6 results
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14ms
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Sources: EU EUDAMED, US FDA
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Status: Completed
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MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display
FDA Enforcement
Class II
·Completed·Barco N.V.·July 17, 2024
ProPlan CMF Patient-Specific Guide, Mandible guides (3A & 3B)-Intended to guide the marking of bone and/or guide surgical instruments in mandibular and maxillofacial surgical procedures. Identification number: SD900.101
FDA Enforcement
Class II
·Completed·Materialise N.V.·August 9, 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 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
ProPlan CMF Patient-Specific Guide, Mandible guides (3A & 3B)-Intended to guide the marking of bone and/or guide surgical instruments in mandibular and maxillofacial surgical procedures. Identification number: SD900.101
FDA Recall
Completed
·Materialise N.V. Technologielaan 15 Heverlee Belgium·Product code JEY·June 19, 2023
MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display
FDA Recall
Completed
·Barco N.V. President Kennedypark 35 Kortrijk Belgium·Product code DXJ·April 24, 2024