刺激器，骨生長，非侵入式
PMA 核准號：P030034 · 2022-06-14
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器材摘要
Stimulator, bone growth, non-invasive is the device name listed in this FDA 510(k) record. The listed applicant is Orthofix, Inc.. It received FDA 510(k) clearance on 2022-06-14. The device is classified under product code LOF. It was reviewed by the OR advisory panel.
常見問題
What is the Stimulator, bone growth, non-invasive?
Stimulator, bone growth, non-invasive is a medical device that received FDA 510(k) clearance on 2022-06-14. The listed applicant is Orthofix, Inc..
When did Stimulator, bone growth, non-invasive receive FDA 510(k) clearance?
The clearance date for Stimulator, bone growth, non-invasive can be found in the official FDA records.
Who is the listed applicant for Stimulator, bone growth, non-invasive?
The FDA 510(k) record lists Orthofix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stimulator, bone growth, non-invasive?
The FDA product code for Stimulator, bone growth, non-invasive is LOF.
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官方來源
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