CORTAC
Model 2110-20-076 · PMT CORPORATION · DI 00650551000211
GYC — Electrode, Cortical · Class II · 21 CFR 882.1310
UDILibrary device dossier · generated 2026-09-11 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.
Recall history (0)
No recalls linked in the loaded window.
Adverse-event reports — MAUDE (0)
Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.
| Month | This device (reports) | Product-code average (reports per device) |
|---|---|---|
| 2020-01 | 0 | 1 |
| 2022-10 | 0 | 3 |
| 2023-08 | 0 | 1 |
| 2024-05 | 0 | 3 |
| 2024-12 | 0 | 6 |
| 2025-09 | 0 | 3 |
Regulatory clearances
- None linked in the loaded window.
Predicate lineage
K082474 — cited as predicate by K110967, K180290, K192764
Lineage extracted from public 510(k) summary text (heuristic).
Manufacturer compliance record — PMT CORPORATION
- Warning Letter 2009-12-03 PMT Corporation
- Warning Letter 2009-12-03 PMT Corporation
- VAI 2024-02-15 PMT Corporation · 4 citations
- VAI 2024-02-15 PMT Corporation · 4 citations
- NAI 2017-03-23 PMT Corporation · 2 citations
- NAI 2017-03-23 PMT Corporation · 2 citations
- NAI 2013-06-06 PMT Corporation · 7 citations
- NAI 2013-06-06 PMT Corporation · 7 citations
- VAI 2010-07-16 PMT Corporation · 0 citations
- VAI 2010-07-16 PMT Corporation · 0 citations