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Home » FDA approves next-gen intrathecal drug delivery system from Medtronic

FDA approves next-gen intrathecal drug delivery system from Medtronic

October 10, 2023 By Sean Whooley

Medtronic SynchroMed III drug delivery system
The SynchroMed III system. [Image courtesy of Medtronic]
Medtronic (NYSE:MDT) announced today that the FDA approved its next-generation SynchroMed III intrathecal drug delivery system.

The medtech giant designed SynchroMed III to treat patients with chronic pain, cancer pain and severe spasticity. The targeted drug delivery (TDD) system alleviates symptoms by delivering medication directly to the fluid surrounding the spinal cord.

SynchroMed III builds upon the previous SynchroMed II system, featuring a new “refill only” physician workflow. This enables more efficient programming, while improved electronics feature firmware capable of updates post-implant. Additionally, the system has other protections for patient data through enhanced cybersecurity.

Medtronic said its system also carries forward several mid-generation durable design enhancements from the previous generation.

Get the full story at our sister site, Drug Delivery Business News.

Filed Under: Drug Pumps, Drug-Device Combinations, Food & Drug Administration (FDA), Pain Management, Regulatory/Compliance, Spine Tagged With: FDA, Medtronic

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About Sean Whooley

Sean Whooley is an associate editor who mainly produces work for MassDevice, Medical Design & Outsourcing and Drug Delivery Business News. He received a bachelor's degree in multiplatform journalism from the University of Maryland, College Park. You can connect with him on LinkedIn or email him at [email protected].

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