FDA 510(k)

PlasmaBlade T

K-Number: K170610 · 2017-04-13

Decision Date2017-04-13

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

PlasmaBlade T is a medical device manufactured by Medtronic Advanced Energy. It received FDA 510(k) clearance on 2017-04-13 under approval number K170610. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PlasmaBlade T?

PlasmaBlade T is a medical device that received FDA 510(k) clearance on 2017-04-13. It is manufactured by Medtronic Advanced Energy. The 510(k) number is K170610.

When was PlasmaBlade T approved by the FDA?

PlasmaBlade T received FDA 510(k) clearance on 2017-04-13, under approval number K170610.

What company makes PlasmaBlade T?

PlasmaBlade T is manufactured by Medtronic Advanced Energy.

What is the FDA product code for PlasmaBlade T?

The FDA product code for PlasmaBlade T is GEI.

Other Devices by Medtronic Advanced Energy

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.