Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA PMA

Stimulator, bone growth, non-invasive

PMA Number: P230025 · 2024-11-12

ApplicantXstim, Inc.
Decision Date2024-11-12
PMA NumberP230025
Product CodeLOF
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOR

Device Summary

Stimulator, bone growth, non-invasive is the device name listed in this FDA 510(k) record. The listed applicant is Xstim, Inc.. It received FDA 510(k) clearance on 2024-11-12. The device is classified under product code LOF. It was reviewed by the OR advisory panel.

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 2024-11-12. The listed applicant is Xstim, 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 Xstim, 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.

↑