FDA Device Establishments · JSON-LD · Markdown
FEI 1000432246 · Manufacture Medical Device · Status: Active
| FEI Number | 1000432246 |
|---|---|
| Owner / Operator | Medtronic, Inc. (#2112641) |
| Address | 5389 route de Strasbourg - Vancia, RILLIEUX-LA-PAPE Auvergne-Rhone-Alpes, 69140, FR |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | NKG, KWP |
| Regulation § (21 CFR) | 888.3075, 888.3050 |
| Proprietary names | PASS OCT Patient Specific Rods |
Source: openFDA. Public-domain (CC0).