FDA 510(k)

MEDTRONIC DUAL CHANNEL SPINAL CORD STIM

K-Number: K812155 · 1981-10-08

Decision Date1981-10-08

Product CodeGZB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC DUAL CHANNEL SPINAL CORD STIM is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1981-10-08 under 510(k) number K812155. 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 DUAL CHANNEL SPINAL CORD STIM?

MEDTRONIC DUAL CHANNEL SPINAL CORD STIM is a medical device that received FDA 510(k) clearance on 1981-10-08. The listed applicant is Medtronic Vascular. The 510(k) number is K812155.

When did MEDTRONIC DUAL CHANNEL SPINAL CORD STIM receive FDA 510(k) clearance?

MEDTRONIC DUAL CHANNEL SPINAL CORD STIM received FDA 510(k) clearance on 1981-10-08, under 510(k) number K812155.

Who is the listed applicant for MEDTRONIC DUAL CHANNEL SPINAL CORD STIM?

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 DUAL CHANNEL SPINAL CORD STIM?

The FDA product code for MEDTRONIC DUAL CHANNEL SPINAL CORD STIM 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.