FDA Device Establishments · JSON-LD · Markdown

NUVASIVE, INC.

FEI 3002980729 · Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active

FEI Number3002980729
Owner / OperatorNUVASIVE, INC. (#9036345)
Address7475 Lusk Blvd, SAN DIEGO, CA, US
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)KWP, NKG
Regulation § (21 CFR)888.3050, 888.3075
Proprietary namesNuVasive RELINE Cervical System

External sources

Source: openFDA. Public-domain (CC0).