Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
MJW · Predicate Candidate Screening
2 FDA 510(k) clearances under this product code; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K033046 | SUBTALAR PEG IMPLANT | Nexa Orthopedics, Inc. | 2003-12-23 | 85 | 0 |
| K922292 | LUNDEEN SUBTALAR PEG IMPLANT | Sgarlato Laboratories, Inc. | 1992-10-23 | 161 | 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