LDR closer to FDA approval for cervical disc device

11/8/2012 | BeckersOrthopedicAndSpine.com

The FDA has issued an approvable letter to LDR for its Mobi-C system, a metal and polyethylene mobile bearing prosthetic device tailored for use in one- to two-level cervical disc replacement procedures. The company expects to satisfy the remaining approval requirements and release the device in the U.S. next year.

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