Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Xtrak Medical, Inc. · 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) |
|---|---|---|---|---|---|
| K032660 | XTRAK SUPPORT CATHETER | Xtrak Medical, Inc. | 2003-10-29 | 62 | 0 |
| K021641 | XTD THROMBECTOMY CATHETER, XX CM | Xtrak Medical, Inc. | 2002-07-26 | 67 | 1 |
| K013473 | XTD THROMBECTOMY CATHETER, XX CM, MODEL# CT000500X; XTD CONT | Xtrak Medical, Inc. | 2002-03-06 | 139 | 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