Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Life Spine, LLC · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K133564 | MODIFICATION TO NAUTILUS SPINAL SYSTEM | Life Spine, LLC | 2014-02-19 | 91 | 0 |
| K040844 | LIFE SPINE NEO ANTERIOR CERVICAL PLATE SYSTEM | Life Spine, LLC | 2004-07-23 | 113 | 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