肯特羅斯賓 PSS 椎板螺釘系統
K 號：K220486 · 2022-07-22
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器材摘要
Kentrospine PSS Pedicle Screw System is the device name listed in this FDA 510(k) record. The listed applicant is Rivarp Medical Private Limited. It received FDA 510(k) clearance on 2022-07-22 under 510(k) number K220486. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Kentrospine PSS Pedicle Screw System?
Kentrospine PSS Pedicle Screw System is a medical device that received FDA 510(k) clearance on 2022-07-22. The listed applicant is Rivarp Medical Private Limited. The 510(k) number is K220486.
When did Kentrospine PSS Pedicle Screw System receive FDA 510(k) clearance?
Kentrospine PSS Pedicle Screw System received FDA 510(k) clearance on 2022-07-22, under 510(k) number K220486.
Who is the listed applicant for Kentrospine PSS Pedicle Screw System?
The FDA 510(k) record lists Rivarp Medical Private Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Kentrospine PSS Pedicle Screw System?
The FDA product code for Kentrospine PSS Pedicle Screw System is NKB.
相關臨床試驗
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相關器械（代碼：NKB）
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
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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