FdaApprovalPulse: records in Minnesota, page 2 of 2

Records 51 to 61 of the 61 newest listed for this hub. Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration).

RecordProductApprovalDecided
Medtronic, Inc.Affera Ablation SystemPMA supplement (device change)2026-05-28
Medtronic Cardiac Rhythm Disease ManagementSelectSecure Lead Model 3830PMA supplement (device change)2026-05-28
Envoy Medical CorporationEsteem®PMA supplement (device change)2026-05-21
Medtronic, Inc.Activa™ Deep Brain Stimulation Therapy System, Percept™ PC BrainSense™PMA supplement (device change)2026-05-20
Boston Scientific CorpWATCHMAN FLX™ Left Atrial Appendage Closure Device with Delivery System; WATCHMAN FLX™ Pro Left Atrial Appendage ClosurePMA supplement (device change)2026-05-18
Medtronic, Inc.Sphere-9 Catheter and Affera Ablation SystemPMA supplement (device change)2026-05-15
Medtronic, Inc.Percepta Bipolar CRT-P (WlTR0l); Percepta Quadripolar CRT-P (W4TR01); Serena Bipolar CRT-P (WlTR02); Serena QuadripolarPMA supplement (device change)2026-05-14
Medtronic, Inc.Astra S DR MRI IPG (X3DR01);Astra S SR MRI IPG (X3SR01);Astra XT DR MRI IPG (X1DR01); Astra XT SR MRI IPG (X1SR01); AzurPMA supplement (device change)2026-05-14
Medtronic, Inc.CareLink SmartSync Platform Application (M01A01); CareLink SmartSync Common Application (M01A02); CareLink SmartSync HosPMA supplement (device change)2026-05-06
Medtronic, Inc.CareLink SmartSync™ Adapta™ Versa™ Sensia™ Application (D00U014)PMA supplement (device change)2026-05-06
Boston Scientific CorporationRanger™ Paclitaxel-Coated PTA Balloon CatheterPMA supplement (device change)2026-05-01

All FdaApprovalPulse record reports

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