Medical Device Manufacturer · US , San Diego , CA

Medtronic Versaflex, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1989

Total

Cleared

Denied

Medtronic Versaflex, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 2 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Medtronic Versaflex, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Medtronic Versaflex, Inc.

2 devices

1-2 of 2