Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medmetric Corp. · Predicate Candidate Screening
8 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
41 daysmedian FDA review time
240 days90th percentile
8clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K943197 | KT1000/S KNEE LIGAMENT ARTHROMETER | Medmetric Corp. | 1995-03-02 | 240 | 0 |
| K942059 | KT2000 KNEE LIGAMENT ARTHROMETER | Medmetric Corp. | 1994-09-20 | 144 | 0 |
| K904823 | FLEXERCYCLE | Medmetric Corp. | 1991-01-30 | 97 | 0 |
| K904898 | TORQUE FRAME QTF1000 | Medmetric Corp. | 1990-11-28 | 29 | 0 |
| K854254 | TENSION-ISOMETER | Medmetric Corp. | 1985-11-15 | 24 | 0 |
| K812806 | KT-1000 DEVICE | Medmetric Corp. | 1981-11-10 | 35 | 0 |
| K812713 | DRAWER TEST | Medmetric Corp. | 1981-11-05 | 41 | 0 |
| K801572 | SURG-ASSIST | Medmetric Corp. | 1980-08-04 | 26 | 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