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Cement Restrictor
Model TPA-18 · TECRES SPA · DI 08031497001401
JDK — Prosthesis, Hip, Cement Restrictor · Class II · 21 CFR 878.3300
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.
Monthly adverse-event reports for this device versus the product-code average.
Month
This device (reports)
Product-code average (reports per device)
2019-02
0
1
2019-07
0
1
2019-08
0
1
2019-10
0
3
2021-06
0
3
2021-07
0
2
2022-07
0
1
2023-10
0
2
2024-02
0
2
2024-04
0
2
2024-10
0
1
2025-01
0
1
2025-03
0
2
2025-04
0
1
2025-06
0
1
2025-07
0
1
2026-05
0
1
This device (reports/month)Average device in JDK (reports/device/month)
Regulatory clearances
None linked in the loaded window.
Predicate lineage
K021765 — cited as predicate by K210062
Lineage extracted from public 510(k) summary text (heuristic).