刺激器，侵入性骨生長
PMA 核准號：P850035 · 2024-09-20
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器材摘要
Stimulator, invasive bone growth is the device name listed in this FDA 510(k) record. The listed applicant is Ahp Eos Buyer, Inc.. It received FDA 510(k) clearance on 2024-09-20. The device is classified under product code LOE. It was reviewed by the OR advisory panel.
常見問題
What is the Stimulator, invasive bone growth?
Stimulator, invasive bone growth is a medical device that received FDA 510(k) clearance on 2024-09-20. The listed applicant is Ahp Eos Buyer, Inc..
When did Stimulator, invasive bone growth receive FDA 510(k) clearance?
The clearance date for Stimulator, invasive bone growth can be found in the official FDA records.
Who is the listed applicant for Stimulator, invasive bone growth?
The FDA 510(k) record lists Ahp Eos Buyer, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stimulator, invasive bone growth?
The FDA product code for Stimulator, invasive bone growth is LOE.
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官方來源
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