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FDA 510(k)

PERIPHERAL NERVE STIMULATION

K-Number: K982902 · 1998-11-10

ApplicantMedtronic Vascular
Decision Date1998-11-10
Product CodeGZF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PERIPHERAL NERVE STIMULATION is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1998-11-10 under 510(k) number K982902. The device is classified under product code GZF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIPHERAL NERVE STIMULATION?

PERIPHERAL NERVE STIMULATION is a medical device that received FDA 510(k) clearance on 1998-11-10. The listed applicant is Medtronic Vascular. The 510(k) number is K982902.

When did PERIPHERAL NERVE STIMULATION receive FDA 510(k) clearance?

PERIPHERAL NERVE STIMULATION received FDA 510(k) clearance on 1998-11-10, under 510(k) number K982902.

Who is the listed applicant for PERIPHERAL NERVE STIMULATION?

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 PERIPHERAL NERVE STIMULATION?

The FDA product code for PERIPHERAL NERVE STIMULATION is GZF.

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Related Devices (Code: GZF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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