Stimulator, bone growth, non-invasive
PMA Number: P850022 · 2024-02-29
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Device Summary
Frequently Asked Questions
What is the Stimulator, bone growth, non-invasive?
Stimulator, bone growth, non-invasive is a medical device that received FDA 510(k) clearance on 2024-02-29. The listed applicant is Ahp Eos Buyer, 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 Ahp Eos Buyer, 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.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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