FDA 510(k)

脊椎CAMP™

K 號：K221632 · 2022-10-18

決定日期2022-10-18

產品代碼QIH

諮詢委員會RA

決定相當於

器材摘要

Spine CAMP™ is the device name listed in this FDA 510(k) record. The listed applicant is Medical Metrics, Inc.. It received FDA 510(k) clearance on 2022-10-18 under 510(k) number K221632. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Spine CAMP™?

Spine CAMP™ is a medical device that received FDA 510(k) clearance on 2022-10-18. The listed applicant is Medical Metrics, Inc.. The 510(k) number is K221632.

When did Spine CAMP™ receive FDA 510(k) clearance?

Spine CAMP™ received FDA 510(k) clearance on 2022-10-18, under 510(k) number K221632.

Who is the listed applicant for Spine CAMP™?

The FDA 510(k) record lists Medical Metrics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Spine CAMP™?

The FDA product code for Spine CAMP™ is QIH.

其他以 Medical Metrics, Inc. 為申請人之記錄

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K231668脊椎CAMP™（1.1）

相關器械（代碼：QIH）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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