The Heart Valve Div. Medtronic Cardiovascular Surg

The Heart Valve Div. Medtronic Cardiovascular Surg holds 5 FDA 510(k) medical device clearances, first cleared 1991, most recent 1998.

Top product codes for The Heart Valve Div. Medtronic Cardiovascular Surg

KRH — Cardiovascular3 devices
LDF — Cardiovascular2 devices

Recent clearances by The Heart Valve Div. Medtronic Cardiovascular Surg

K980534 — DURAN FLEXIBLE ANNULOPLASTY RING MODEL NUMBER H608HCode KRH·1998-04-30
K960356 — POSTERIOR ANNULOPLASTY BAND (MODEL 607)Code KRH·1996-08-27
K944956 — UNIPOLAR PEDIATRIC TEMPORARY PACING LEAD, MODEL 6491Code LDF·1995-07-14
K922269 — UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE, 6493Code LDF·1992-11-23
K914602 — DURAN FLEX ANNULOPLASTY RING/OBTUR H601H, MODIFIEDCode KRH·1991-11-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.