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., part of StrykerLabelled 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 13, 2026, FDA's public records list Spine-Tech, Inc. with 4 510(k) clearances. The most recent is a 510(k) clearance dated Jul 29, 1998: SPINE-TECH SILHOUETTE SPINAL FIXATION SYSTEM.
| Date | Record | Source |
|---|---|---|
| Jul 29, 1998 | SPINE-TECH SILHOUETTE SPINAL FIXATION SYSTEMK980288 · KWP | 510(k) clearances |
| Feb 28, 1997 | SPINE-TECH BONE HARVESTERK970040 · HWE | 510(k) clearances |
| Jul 31, 1995 | SPINE-TECH MODIFIED LAPAROSCOPIC SPINAL FUSION INSTRUMENT SYSTEMK951268 · HRX | 510(k) clearances |
| Oct 4, 1994 | SPINE-TECH LAPAROSCOPIC INSTRUMENTATION SYSTEMK940913 · HRX | 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
