人工脊椎，椎間盤
PMA 核准號：P070001 · 2026-09-09
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器材摘要
Prosthesis, intervertebral disc is the device name listed in this FDA 510(k) record. The listed applicant is Centinel Spine, LLC. It received FDA 510(k) clearance on 2026-09-09. The device is classified under product code MJO. It was reviewed by the OR advisory panel.
常見問題
What is the Prosthesis, intervertebral disc?
Prosthesis, intervertebral disc is a medical device that received FDA 510(k) clearance on 2026-09-09. The listed applicant is Centinel Spine, LLC.
When did Prosthesis, intervertebral disc receive FDA 510(k) clearance?
The clearance date for Prosthesis, intervertebral disc can be found in the official FDA records.
誰是Prosthesis, intervertebral disc的登記申請人？
The FDA 510(k) record lists Centinel Spine, LLC as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼為Prosthesis, intervertebral disc是什麼？
FDA產品代碼為人工關節、椎間盤的Prosthesis為MJO。
相關臨床試驗
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。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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