FDA Device Establishments · JSON-LD · Markdown
FEI 3006172536 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3006172536 |
|---|---|
| Owner / Operator | Wenzel Spine, Inc. (#10030760) |
| Address | 2535 Brockton Dr Ste 450, Austin, TX, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KWP |
| Regulation § (21 CFR) | 888.3050 |
| Proprietary names | PrimaLOK-SP Interspinous Fusion System |
Source: openFDA. Public-domain (CC0).