FDA 510(k)

Supplemental Instrument Trays

K番号: K170939 · 2017-08-08

申請者Nuvasive Specialized Orthopedics, Incorporated

決定日2017-08-08

製品コードKCT

諮問委員会医療機器規制テキストの翻訳は以下の通りです。 HO [翻訳が提供されなかったため、原文の「HO」がそのまま使用されます]

決定Substantially Equivalent

医療機器の概要

Supplemental Instrument Trays is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive Specialized Orthopedics, Incorporated. It received FDA 510(k) clearance on 2017-08-08 under 510(k) number K170939. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Supplemental Instrument Trays?

Supplemental Instrument Trays is a medical device that received FDA 510(k) clearance on 2017-08-08. The listed applicant is Nuvasive Specialized Orthopedics, Incorporated. The 510(k) number is K170939.

When did Supplemental Instrument Trays receive FDA 510(k) clearance?

Supplemental Instrument Trays received FDA 510(k) clearance on 2017-08-08, under 510(k) number K170939.

Who is the listed applicant for Supplemental Instrument Trays?

The FDA 510(k) record lists Nuvasive Specialized Orthopedics, Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Supplemental Instrument Trays?

The FDA product code for Supplemental Instrument Trays is KCT.

申請者としてNuvasive Specialized Orthopedics, Incorporatedを記載するその他の記録

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