FDA 510(k)

neoWave LS Lumbar Straight, neoWave C Cervical, and Ti3D Cervical

K番号: K222988 · 2023-09-01

決定日2023-09-01

製品コードODP

諮問委員会医薬品機器規制テキストの翻訳は以下の通りです。 [原文] OR [翻訳] OR 注：原文が具体的な内容を含んでいないため、翻訳は単なる「OR」のままです。

決定大幅同等

医療機器の概要

neoWave LS Lumbar Straight, neoWave C Cervical, and Ti3D Cervical is the device name listed in this FDA 510(k) record. The listed applicant is Ht Medical D.B.A. Xenix Medical. It received FDA 510(k) clearance on 2023-09-01 under 510(k) number K222988. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the neoWave LS Lumbar Straight, neoWave C Cervical, and Ti3D Cervical?

neoWave LS Lumbar Straight, neoWave C Cervical, and Ti3D Cervical is a medical device that received FDA 510(k) clearance on 2023-09-01. The listed applicant is Ht Medical D.B.A. Xenix Medical. The 510(k) number is K222988.

When did neoWave LS Lumbar Straight, neoWave C Cervical, and Ti3D Cervical receive FDA 510(k) clearance?

neoWave LS Lumbar Straight, neoWave C Cervical, and Ti3D Cervical received FDA 510(k) clearance on 2023-09-01, under 510(k) number K222988.

Who is the listed applicant for neoWave LS Lumbar Straight, neoWave C Cervical, and Ti3D Cervical?

The FDA 510(k) record lists Ht Medical D.B.A. Xenix Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for neoWave LS Lumbar Straight, neoWave C Cervical, and Ti3D Cervical?

The FDA product code for neoWave LS Lumbar Straight, neoWave C Cervical, and Ti3D Cervical is ODP.

申請者としてHt Medical D.B.A. Xenix Medicalを記載するその他の記録

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