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Port & Catheter, Implanted, Subcutaneous, Intraventricular

FDA product code LKG · Class 2 · Neurology

106

Registered devices

113

Adverse events

0

Recalls

8

510(k) clearances

Devices with this code

Innervision — MEDTRONIC PS MEDICAL, INC.N/A — MEDTRONIC PS MEDICAL, INC.N/A — MEDTRONIC PS MEDICAL, INC.Innervision — MEDTRONIC PS MEDICAL, INC.NA — MEDTRONIC PS MEDICAL, INC.Innervision — MEDTRONIC PS MEDICAL, INC.Innervision — MEDTRONIC PS MEDICAL, INC.NA — MEDTRONIC PS MEDICAL, INC.NA — MEDTRONIC PS MEDICAL, INC.Innervision — MEDTRONIC PS MEDICAL, INC.N/A — MEDTRONIC PS MEDICAL, INC.NA — MEDTRONIC POWERED SURGICAL SOLUTIONS Innervision — MEDTRONIC PS MEDICAL, INC.N/A — MEDTRONIC PS MEDICAL, INC.Innervision — MEDTRONIC PS MEDICAL, INC.NA — MEDTRONIC PS MEDICAL, INC.N/A — MEDTRONIC PS MEDICAL, INC.N/A — MEDTRONIC PS MEDICAL, INC.N/A — MEDTRONIC PS MEDICAL, INC.NA — MEDTRONIC PS MEDICAL, INC.NA — MEDTRONIC PS MEDICAL, INC.NA — MEDTRONIC PS MEDICAL, INC.Innervision — MEDTRONIC PS MEDICAL, INC.NA — MEDTRONIC PS MEDICAL, INC.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.