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FDA PMA

Stimulator, invasive bone growth

PMA Number: P850035 · 2024-09-20

ApplicantAhp Eos Buyer, Inc.
Decision Date2024-09-20
PMA NumberP850035
Product CodeLOE
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOR

Device Summary

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.

Frequently Asked Questions

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.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT04745156A Study Using Brain Stimulation and Behavioral Therapy to Increase Extent of Resection in Low-Grade GliomasNOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED

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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