Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Pinnacle Spine Group with 13 510(k) clearances. The most recent is a 510(k) clearance dated Dec 14, 2017: InFill® Interbody Fusion Device.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Dec 14, 2017 | InFill® Interbody Fusion DeviceK172349 · MAX | 510(k) clearances |
| Nov 19, 2015 | InFill Interbody Fusion DeviceK152259 · MAX | 510(k) clearances |
| Jul 14, 2015 | InFill Interbody Fusion DevicesK151184 · MAX | 510(k) clearances |
| Apr 3, 2015 | InFill Interbody Fusion DevicesK150206 · MAX | 510(k) clearances |
| Dec 17, 2014 | InFill Graft Delivery SystemK143488 · FMF | 510(k) clearances |
| Dec 2, 2014 | PGS 5.5 MM CANNULATED PEDICLE SCREWK141282 · NKB | 510(k) clearances |
| May 5, 2014 | INFILL CERVICALK140066 · ODP | 510(k) clearances |
| Mar 31, 2014 | INFILL 41-TLIF CONVEX OBLIQUE DEVICE, INFILL 43-TLIF CONTOUR OBLIQUE, INFILL 44-TLIF CONTOUR OBLIQUE AND THE INFILL 60K133721 · MAX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
