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FDA PMA

Cochlear implant with combined electrical stimulation and acoustic amplification

PMA Number: P130016 · 2026-09-28

Decision Date2026-09-28
PMA NumberP130016
Product CodePGQ
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeEN

Device Summary

Cochlear implant with combined electrical stimulation and acoustic amplification is the device name listed in this FDA 510(k) record. The listed applicant is Cochlear Americas. It received FDA 510(k) clearance on 2026-09-28. The device is classified under product code PGQ. It was reviewed by the EN advisory panel.

Frequently Asked Questions

What is the Cochlear implant with combined electrical stimulation and acoustic amplification?

Cochlear implant with combined electrical stimulation and acoustic amplification is a medical device that received FDA 510(k) clearance on 2026-09-28. The listed applicant is Cochlear Americas.

When did Cochlear implant with combined electrical stimulation and acoustic amplification receive FDA 510(k) clearance?

The clearance date for Cochlear implant with combined electrical stimulation and acoustic amplification can be found in the official FDA records.

Who is the listed applicant for Cochlear implant with combined electrical stimulation and acoustic amplification?

The FDA 510(k) record lists Cochlear Americas as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cochlear implant with combined electrical stimulation and acoustic amplification?

The FDA product code for Cochlear implant with combined electrical stimulation and acoustic amplification is PGQ.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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