Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Depuy Spine · 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) |
|---|---|---|---|---|---|
| K222276 | CONDUIT Cages; FIBERGRAFT BG Putty | Depuy Spine | 2022-10-15 | 78 | 0 |
| K101923 | CONCORDE CURVE SYSTEM | Depuy Spine | 2010-12-01 | 145 | 0 |
| K082128 | DEPUY SPINE LATERAL CAGE SYSTEM | Depuy Spine | 2008-11-14 | 108 | 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