Accu-Joint
Model AJPI-16-15 · Accufix Surgical, Inc. · DI 00850044114207
KWD — Prosthesis, Toe, Hemi-, Phalangeal · Class II · 21 CFR 888.3730
UDILibrary device dossier · generated 2026-09-15 · 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) |
|---|---|---|
| 2019-06 | 0 | 3 |
| 2019-07 | 0 | 1 |
| 2022-05 | 0 | 1 |
| 2023-02 | 0 | 2.5 |
| 2023-04 | 0 | 3 |
| 2023-06 | 0 | 3 |
| 2023-07 | 0 | 3 |
| 2023-10 | 0 | 2 |
| 2024-02 | 0 | 4 |
| 2024-05 | 0 | 3 |
| 2024-12 | 0 | 2 |
| 2026-04 | 0 | 1 |
| 2026-06 | 0 | 1 |
Regulatory clearances
- None linked in the loaded window.
Predicate lineage
K200951 — cites (transitively): K023684 (d1), K070052 (d1), K102401 (d1), K121973 (d1), K190543 (d1), K031859 (d2), K132496 (d2), K152454 (d2), K072251 (d3), K102549 (d3), K131377 (d3), K904724 (d4), K924724 (d4), K113752 (d4), K073065 (d5) — cited as predicate by K240268
Lineage extracted from public 510(k) summary text (heuristic).
Manufacturer compliance record — Accufix Surgical, Inc.
- NAI 2025-04-30 Accufix Surgical, Inc. · 0 citations
- NAI 2025-04-30 Accufix Surgical, Inc. · 0 citations