FDA 510(k)

SPINAL CORD STIMULATION SYS SE-4

K-Number: K833990 · 1984-03-19

Decision Date1984-03-19

Product CodeGZB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

SPINAL CORD STIMULATION SYS SE-4 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1984-03-19 under 510(k) number K833990. 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 SPINAL CORD STIMULATION SYS SE-4?

SPINAL CORD STIMULATION SYS SE-4 is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is Medtronic Vascular. The 510(k) number is K833990.

When did SPINAL CORD STIMULATION SYS SE-4 receive FDA 510(k) clearance?

SPINAL CORD STIMULATION SYS SE-4 received FDA 510(k) clearance on 1984-03-19, under 510(k) number K833990.

Who is the listed applicant for SPINAL CORD STIMULATION SYS SE-4?

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 SPINAL CORD STIMULATION SYS SE-4?

The FDA product code for SPINAL CORD STIMULATION SYS SE-4 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.