Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Depuy Motech Acromed — Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K990148 | STACKABLE CAGE SYSTEM | Depuy Motech Acromed | 1999-09-03 | 227 | 0 |
| K984348 | TIMX LOW BACK SYSTEM | Depuy Motech Acromed | 1999-01-20 | 47 | 0 |
| K984350 | VSP SYSTEM | Depuy Motech Acromed | 1999-01-20 | 47 | 0 |
| K982443 | DOC VENTRAL CERVICAL STABILIZATION SYSTEM | Depuy Motech Acromed | 1998-07-29 | 15 | 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