Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Axis Orthopaedics — 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) |
|---|---|---|---|---|---|
| K181140 | Axis Chena Cervical PEEK Spacer System | Axis Orthopaedics | 2018-11-16 | 200 | 0 |
| K180301 | AXIS 5.5 Lumbar Pedicle Screw System | Axis Orthopaedics | 2018-04-10 | 67 | 0 |
| K173867 | Axis Anterior Cervical Plate System | Axis Orthopaedics | 2018-04-05 | 106 | 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