FDA 510(k)

maxmorespine Bipolar Electrodes

K-Number: K211173 · 2022-06-23

Decision Date2022-06-23

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

maxmorespine Bipolar Electrodes is a medical device manufactured by Hoogland Spine Products, GmbH. It received FDA 510(k) clearance on 2022-06-23 under approval number K211173. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the maxmorespine Bipolar Electrodes?

maxmorespine Bipolar Electrodes is a medical device that received FDA 510(k) clearance on 2022-06-23. It is manufactured by Hoogland Spine Products, GmbH. The 510(k) number is K211173.

When was maxmorespine Bipolar Electrodes approved by the FDA?

maxmorespine Bipolar Electrodes received FDA 510(k) clearance on 2022-06-23, under approval number K211173.

What company makes maxmorespine Bipolar Electrodes?

maxmorespine Bipolar Electrodes is manufactured by Hoogland Spine Products, GmbH.

What is the FDA product code for maxmorespine Bipolar Electrodes?

The FDA product code for maxmorespine Bipolar Electrodes is GEI.

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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.