# NUVASIVE, INC.

FEI: 3002980729
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: NUVASIVE, INC. (#9036345)

Address: 7475 Lusk Blvd, SAN DIEGO, CA, US



## Products

Total registered: 2
Top product codes: KWP, NKG
Regulation §: 888.3050, 888.3075

Proprietary names: NuVasive RELINE Cervical System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002980729%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002980729