Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Intrauma S.P.A — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K252959 | WRISTAR MultiAx Distal Radius Kit | Intrauma S.P.A | 2025-11-12 | 57 | 0 |
| K230623 | KITE Distal Fibula Kit | Intrauma S.P.A | 2023-09-01 | 179 | 0 |
| K201147 | Elos® Intramedullary Nailing System | Intrauma S.P.A | 2021-07-19 | 446 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda