Medtronic, Inc.
FDA 510(k) medical device clearances.
Clearances by Medtronic, Inc. — page 3
201–210 of 210- K080509 — CARDIOBLATE 68000 GNERATOR, BP2 SURGICAL ABLATION DEVICE, LP SURGICAL ABLATION DEVICE, GEMINI-SSURGICAL ABLATION DEVICE
- K073324 — MEDTRONIC PROFILE 3D ANNULOPLASTY RING, MODEL 680R
- K071641 — REVEAL XT; INSERTABLE CARDIAC MONITOR (MODEL 9529), PATIENT ASSISTANT (MODEL 9539)
- K071655 — REVEAL DX INSERTABLE CARDIAC MONITOR, REVEAL PATIENT ASSISTANT, MODEL(S) 9528,9538
- K072990 — GUARDWIRE TEMPORARY OCCLUSION AND ASPIRATION SYSTEM- CAROTID
- K072155 — PIONEER CATHETER
- K070886 — MEROGEL INJECTABLE BIORESORBABLE STENT
- K062041 — MODEL 3875 1 X 8 SC TEST STIMULATION LEAD
- K060400 — CARDIOBLATE SURGICAL ABLATION GENERATOR, MODEL 68000; CARDIOBLATE BP2 SURGICAL ABLATION DEVICE, MODEL 60831; CARDIOBLAT
- K810677 — MODELS 5976/5977 PACEMAKER PULSE GENER
Data sourced from openFDA. This site is unofficial and independent of the FDA.