Unnamed device
Model 174332987 · DEPUY SPINE, LLC · DI 10705034018348
EZX — Mesh, Surgical, Metal · Class II · 21 CFR 878.3300
UDILibrary device dossier · generated 2026-09-06 · 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) |
|---|---|---|
| 2019-04 | 0 | 1 |
| 2019-10 | 0 | 1 |
| 2019-11 | 0 | 1 |
| 2020-04 | 0 | 1 |
| 2021-10 | 0 | 1 |
| 2021-11 | 0 | 1 |
Regulatory clearances
- None linked in the loaded window.
Predicate lineage
K900138 — cited as predicate by K173787
Lineage extracted from public 510(k) summary text (heuristic).
Manufacturer compliance record — DEPUY SPINE, LLC
- NAI 2019-04-18 DePuy Spine, Inc. · 0 citations
- NAI 2019-04-18 DePuy Spine, Inc. · 0 citations
- NAI 2017-06-16 DePuy Spine, Inc. · 0 citations
- NAI 2017-06-16 DePuy Spine, Inc. · 0 citations
- NAI 2012-06-11 DePuy Spine, Inc. · 0 citations
- NAI 2012-06-11 DePuy Spine, Inc. · 0 citations
- NAI 2012-03-06 Depuy Spine Inc · 0 citations
- VAI 2012-02-10 DePuy Spine, Inc. · 2 citations
- VAI 2012-02-10 DePuy Spine, Inc. · 2 citations