FDA 510(k)

ミミクス・サスケトニック・プランナー

K番号: K251964 · 2026-03-12

決定日2026-03-12

製品コードLLZ

諮問委員会RA （注：由于原文中未提供具体的医疗设备监管文本内容，因此无法进行翻译。请提供具体的文本内容以便进行翻译。）

決定大幅同等

医療機器の概要

Mimics Thoracic Planner is the device name listed in this FDA 510(k) record. The listed applicant is Materialise NV. It received FDA 510(k) clearance on 2026-03-12 under 510(k) number K251964. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Mimics Thoracic Planner?

Mimics Thoracic Planner is a medical device that received FDA 510(k) clearance on 2026-03-12. The listed applicant is Materialise NV. The 510(k) number is K251964.

When did Mimics Thoracic Planner receive FDA 510(k) clearance?

Mimics Thoracic Planner received FDA 510(k) clearance on 2026-03-12, under 510(k) number K251964.

Who is the listed applicant for Mimics Thoracic Planner?

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

What is the FDA product code for Mimics Thoracic Planner?

The FDA product code for Mimics Thoracic Planner is LLZ.

申請者としてMaterialise NVを記載するその他の記録

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