StimQ Peripheral Nerve Stimulator (PNS) System— 510(k) K152178

Substantially Equivalent

Stimq, LLC

FDA 510(k) clearance K152178 for StimQ Peripheral Nerve Stimulator (PNS) System, Substantially Equivalent on 2016-03-11. Applicant: Stimq, LLC. Device class: 2.

Clearance details

Applicant
Stimq, LLC
Product code
Code GZF
Device class
Class 2
Regulation
21 CFR 882.5870
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Fort Lauderdale, FL, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code GZF

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Adverse events under product code GZF

product code GZF
Death
10
Injury
2,410
Other
1
Total
2,421

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K152178

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K152178.

Data sourced from openFDA. This site is unofficial and independent of the FDA.