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FDA PMA

Stimulator, tibial, electrical, implantable, for urinary incontinence

PMA Number: P200036 · 2026-09-09

Decision Date2026-09-09
PMA NumberP200036
Product CodeQPT
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeGU

Device Summary

Stimulator, tibial, electrical, implantable, for urinary incontinence is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2026-09-09. The device is classified under product code QPT. It was reviewed by the GU advisory panel.

Frequently Asked Questions

What is the Stimulator, tibial, electrical, implantable, for urinary incontinence?

Stimulator, tibial, electrical, implantable, for urinary incontinence is a medical device that received FDA 510(k) clearance on 2026-09-09. The listed applicant is Boston Scientific Corporation.

When did Stimulator, tibial, electrical, implantable, for urinary incontinence receive FDA 510(k) clearance?

The clearance date for Stimulator, tibial, electrical, implantable, for urinary incontinence can be found in the official FDA records.

Who is the listed applicant for Stimulator, tibial, electrical, implantable, for urinary incontinence?

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

What is the FDA product code for Stimulator, tibial, electrical, implantable, for urinary incontinence?

The FDA product code for Stimulator, tibial, electrical, implantable, for urinary incontinence is QPT.

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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