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FDA 510(k)

MULTISTIM LAMINECTOMY ELECTRODE

K-Number: K853643 · 1985-11-14

ApplicantNeuromed, Inc.
Decision Date1985-11-14
Product CodeGZB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MULTISTIM LAMINECTOMY ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Neuromed, Inc.. It received FDA 510(k) clearance on 1985-11-14 under 510(k) number K853643. 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 MULTISTIM LAMINECTOMY ELECTRODE?

MULTISTIM LAMINECTOMY ELECTRODE is a medical device that received FDA 510(k) clearance on 1985-11-14. The listed applicant is Neuromed, Inc.. The 510(k) number is K853643.

When did MULTISTIM LAMINECTOMY ELECTRODE receive FDA 510(k) clearance?

MULTISTIM LAMINECTOMY ELECTRODE received FDA 510(k) clearance on 1985-11-14, under 510(k) number K853643.

Who is the listed applicant for MULTISTIM LAMINECTOMY ELECTRODE?

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

What is the FDA product code for MULTISTIM LAMINECTOMY ELECTRODE?

The FDA product code for MULTISTIM LAMINECTOMY ELECTRODE is GZB.

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Related Devices (Code: GZB)

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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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