FDA 510(k)

Longeviti ClearFit™ オートセット・スカル・イムプラント

K番号: K212058 · 2021-09-08

決定日2021-09-08

製品コードGXN

諮問委員会Please provide the source text to translate.

決定大幅同等

医療機器の概要

Longeviti ClearFit™ OTS Cranial Implants is the device name listed in this FDA 510(k) record. The listed applicant is Longeviti Neuro Solutions, LLC. It received FDA 510(k) clearance on 2021-09-08 under 510(k) number K212058. The device is classified under product code GXN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Longeviti ClearFit™ OTS Cranial Implants?

Longeviti ClearFit™ OTS Cranial Implants is a medical device that received FDA 510(k) clearance on 2021-09-08. The listed applicant is Longeviti Neuro Solutions, LLC. The 510(k) number is K212058.

When did Longeviti ClearFit™ OTS Cranial Implants receive FDA 510(k) clearance?

Longeviti ClearFit™ OTS Cranial Implants received FDA 510(k) clearance on 2021-09-08, under 510(k) number K212058.

Who is the listed applicant for Longeviti ClearFit™ OTS Cranial Implants?

The FDA 510(k) record lists Longeviti Neuro Solutions, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Longeviti ClearFit™ OTS Cranial Implants?

The FDA product code for Longeviti ClearFit™ OTS Cranial Implants is GXN.

申請者としてLongeviti Neuro Solutions, LLCを記載するその他の記録

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公式ソース

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