Medtronic, Inc. Receives FDA Approval for CapSureFix Pacing Lead, Model 4068

Summary

The US Food and Drug Administration (FDA) has approved Medtronic, Inc.'s application for premarket approval of the CapSureFix Pacing Lead, Model 4068, under the Federal Food, Drug, and Cosmetic Act, following notification by the FDA's Center for Devices and Radiological Health on March 29, 1996.