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 Spine Smith Partners with 9 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Dec 5, 2012: IN:C2 SPINAL FIXATION SYSTEM.
| Dec 5, 2012 | IN:C2 SPINAL FIXATION SYSTEMK122630 · OVE | 510(k) clearances |
| Oct 11, 2012 | VISUALIF CHALLENGING ACCESS PLATEK122168 · OVD | 510(k) clearances |
| Aug 24, 2012 | Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemental fixation.Class II · Implants were incorrectly laser marked as 23mm instead of 28mm. | Device recalls |
| Sep 30, 2010 | SPINESMITH CYNCH SPINAL SYSTEM - VISUALIF INTERBODY FUSION IMPLANT SYSTEMK102090 · OVD | 510(k) clearances |
| Jul 1, 2010 | SPINESMITH CYNCH SPINAL SYSTEMK101085 · MAX | 510(k) clearances |
| Apr 1, 2009 | SPINESMITH CYNCH SPINAL SYSTEMK090376 · MAX | 510(k) clearances |
| Oct 31, 2008 | SPINESMITH PARTNERS, LP CEQUENCE ANTERIOR CERVICAL PLATE SYSTEMK082821 · KWQ | 510(k) clearances |
| Jul 14, 2008 | SPINESMITH PARTNERS, LP CEQUENCE ANTERIOR CERVICAL PLATE SYSTEMK081132 · KWQ | 510(k) clearances |
| Jul 2, 2008 | SPINESMITH CIMPLICITY SPINAL SYSTEMK080971 · MQP | 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
