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FDA 510(k)

MEDTRONIC M2 MAGNET ADJUSTMENT TOOL

K-Number: K052386 · 2005-12-16

ApplicantMedtronic Neurosurgery
Decision Date2005-12-16
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC M2 MAGNET ADJUSTMENT TOOL is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Neurosurgery. It received FDA 510(k) clearance on 2005-12-16 under 510(k) number K052386. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC M2 MAGNET ADJUSTMENT TOOL?

MEDTRONIC M2 MAGNET ADJUSTMENT TOOL is a medical device that received FDA 510(k) clearance on 2005-12-16. The listed applicant is Medtronic Neurosurgery. The 510(k) number is K052386.

When did MEDTRONIC M2 MAGNET ADJUSTMENT TOOL receive FDA 510(k) clearance?

MEDTRONIC M2 MAGNET ADJUSTMENT TOOL received FDA 510(k) clearance on 2005-12-16, under 510(k) number K052386.

Who is the listed applicant for MEDTRONIC M2 MAGNET ADJUSTMENT TOOL?

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

What is the FDA product code for MEDTRONIC M2 MAGNET ADJUSTMENT TOOL?

The FDA product code for MEDTRONIC M2 MAGNET ADJUSTMENT TOOL is JXG.

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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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