Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Ht Medical, 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) |
|---|---|---|---|---|---|
| K170318 | NeoFuse Ti3D PLIF/TLIF/Cervical Interbody | Ht Medical, LLC | 2017-07-12 | 161 | 0 |
| K170511 | NeoFuse HA Enhanced PLIF/TLIF | Ht Medical, LLC | 2017-04-25 | 63 | 0 |
| K153615 | NeoFuse HA Enhanced PLIF/TLIF | Ht Medical, LLC | 2016-05-06 | 141 | 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