FDA 510(k)

MEDTRONIC MATTRIX 3271/3272 NEUROSTIMULATION SYSTEM

K-Number: K934065 · 1995-02-14

Decision Date1995-02-14

Product CodeGZB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC MATTRIX 3271/3272 NEUROSTIMULATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1995-02-14 under 510(k) number K934065. The device is classified under product code GZB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC MATTRIX 3271/3272 NEUROSTIMULATION SYSTEM?

MEDTRONIC MATTRIX 3271/3272 NEUROSTIMULATION SYSTEM is a medical device that received FDA 510(k) clearance on 1995-02-14. The listed applicant is Medtronic Vascular. The 510(k) number is K934065.

When did MEDTRONIC MATTRIX 3271/3272 NEUROSTIMULATION SYSTEM receive FDA 510(k) clearance?

MEDTRONIC MATTRIX 3271/3272 NEUROSTIMULATION SYSTEM received FDA 510(k) clearance on 1995-02-14, under 510(k) number K934065.

Who is the listed applicant for MEDTRONIC MATTRIX 3271/3272 NEUROSTIMULATION SYSTEM?

The FDA 510(k) record lists Medtronic Vascular as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDTRONIC MATTRIX 3271/3272 NEUROSTIMULATION SYSTEM?

The FDA product code for MEDTRONIC MATTRIX 3271/3272 NEUROSTIMULATION SYSTEM is GZB.

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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.