Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Incite Innovation, LLC · 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) |
|---|---|---|---|---|---|
| K130306 | INCITE ANCHORED CERVICAL INTERBODY DEVICE | Incite Innovation, LLC | 2013-04-11 | 63 | 0 |
| K122008 | INCITE ANCHORED CERVICAL INTERBODY (ACI) FUSION DEVICE | Incite Innovation, LLC | 2012-11-16 | 130 | 0 |
| K093808 | INCITE INNOVATION STAND ALONE INTERBODY FUSION DEVICE | Incite Innovation, LLC | 2010-03-24 | 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