Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Alphatec/Nexmed with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jun 22, 2005: ZODIAC SPINAL FIXATION SYSTEM.
| Jun 22, 2005 | ZODIAC SPINAL FIXATION SYSTEMK050830 · KWP | 510(k) clearances |
| Jun 17, 2005 | ZODIAC SPINAL FIXATION SYSTEMK051286 · MNH | 510(k) clearances |
| Apr 18, 2005 | NOVEL VBR SPINAL SYSTEMK050553 · MQP | 510(k) clearances |
| Mar 14, 2005 | TAMARACK ANTERIOR THORACOLUNBARK050390 · KWQ | 510(k) clearances |
| Feb 18, 2005 | ROC LUMBAR PLATING SYSTEMK050078 · MNH | 510(k) clearances |
| Dec 6, 2004 | NEXFLEX TOTAL HIP SYSTEMK042252 · LPH | 510(k) clearances |
| Oct 27, 2004 | ZODIAC POLYAXIAL SPINAL FIXATION SYSTEMK042673 · KWP | 510(k) clearances |
| Oct 7, 2004 | ALPHATEC FEMORAL TROCHANTERIC NAIL (FTN) SYSTEMK042440 · HSB | 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
