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FDA 510(k)

MEDTRONIC MODEL 7728 NEUROMOD

K-Number: K792311 · 1979-11-21

ApplicantMedtronic Vascular
Decision Date1979-11-21
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC MODEL 7728 NEUROMOD is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1979-11-21 under 510(k) number K792311. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC MODEL 7728 NEUROMOD?

MEDTRONIC MODEL 7728 NEUROMOD is a medical device that received FDA 510(k) clearance on 1979-11-21. The listed applicant is Medtronic Vascular. The 510(k) number is K792311.

When did MEDTRONIC MODEL 7728 NEUROMOD receive FDA 510(k) clearance?

MEDTRONIC MODEL 7728 NEUROMOD received FDA 510(k) clearance on 1979-11-21, under 510(k) number K792311.

Who is the listed applicant for MEDTRONIC MODEL 7728 NEUROMOD?

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 MODEL 7728 NEUROMOD?

The FDA product code for MEDTRONIC MODEL 7728 NEUROMOD is GZJ.

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Related Devices (Code: GZJ)

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Official Source

View on FDA Database →

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

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