Nuvasive - FDA 510(k) Cleared Devices

Nuvasive, is a medical device company headquartered in San Diego, California. The company develops and delivers solutions for spine surgery and orthopedic procedures. NuVasive operates globally with a strong presence across multiple international markets.

The company has received 1 FDA 510(k) clearance from 1 total submission. NuVasive specializes in Orthopedic devices, which represent 100% of its regulatory submissions. The company achieved its first FDA 510(k) clearance in 2024 and remains active in the regulatory space.

NuVasive's cleared portfolio includes advanced surgical technologies and intraoperative neuromonitoring services. The company serves hospitals, surgeons, and patients through industry-leading technology and clinical expertise. NuVasive maintains board-certified specialists and comprehensive training programs to support surgical procedures.

For detailed information on cleared device names, product codes, and clearance dates, explore the full regulatory record.