Las Vegas, NV -- (SBWIRE) -- 12/03/2013 -- Invivo Therapeutics Holdings Corp (OTCMKTS:NVIV) declared that it submitted an application to Food and Drug Administration proposing amendments in the FDA-approved protocol of company.
Invivo stated that the filing also focuses to change the supporting documents that are related to the scaffold program for treating spinal cord injuries. The company is hopeful to receive a response to filing in thirty days. Approval of the proposed alterations is expected to speed up the clinical trial process.
InVivo Therapeutics Holdings Corp. formerly known as Design Source, Inc. is emerging in market of spinal cord treatment. The necessity for Invivo product is high since there are no sufficient solutions for cure of spinal cord injuries. The Company manufactures scaffolding devices that safeguard wounded spinal cord from damaging. Products are fixed in the body through surgery or are injected.
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