Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
KYK · Predicate Candidate Screening
3 FDA 510(k) clearances under this product code; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K880826 | MICROLOC(TM) POROUS COATED UNICONDYLAR KNEE SYSTEM | Johnson & Johnson Professionals, Inc. | 1988-03-14 | 13 | 0 |
| K871118 | MODIFIED TOWNLEY UNICONDYLAR KNEE | Depuy, Inc. | 1987-04-06 | 18 | 0 |
| K851341 | SYNATOMIC VARIABLE FIT TIBIAL PLATEAU | Depuy, Inc. | 1985-07-15 | 103 | 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