Replication Medical Receives CE Mark for GelFix Posterior Spine Distraction Implant

Cranbury, N.J.-based Replication Medical, a developer of proprietary, hydrogel based products for the spine and other surgical applications, has received a CE mark for its GelFix Posterior Spinal Distraction implant, according to a Replication news release.

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The GelFix device is a one-piece posterior spinal implant made from HPAN, a biocompatible hydrogel which exhibits desirable mechanical properties including compressive resistance with a dynamic response, and is used as a spacer between the spinous processes to provide separation and prevent nerve pinching, according to the release. The implant comes in three sizes to fit the typical range of spinal stenosis patients.

The GelFix interspinous implant may not only reduce pain, but may also increase the mobility of the patient, according to the release. “The key to the procedure is the minimally invasive technique which can be used to implant the device. We insert the implant between the appropriate spinous processes and in 8-10 hours, the implant increases in size and gives us the stability that we need,” Carl Lauryssen, MD, one of Replication Medical’s surgeon advisors, said in the release.

Read the release about the GelFix Posterior Spinal Distraction implant.

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