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OsteoFab™ Patient Specific Cranial Device Receives 510(k) Approval
Date:2/18/2013

c industry,” said Scott DeFelice, President and CEO of OPM. “We have sought our first approval within cranial implants because the need was most compelling; however, this is just the beginning. We will now move systematically throughout the body in an effort to deliver improved outcomes at lower overall cost to the patient and healthcare provider.” It is OPM’s strategy to undertake all manufacturing and regulatory activities to support patient specific implant product commercialization. The company is seeking well-qualified partners to bring these technologies to market. In addition to its own devices, the company offers bespoke part production for its customers.

About OPM
OPM operates at the intersection of high performance polymers, Additive Manufacturing technologies, and the creation of structures for the biomedical and aerospace sectors. The firm currently has four operating divisions: Biomedical Devices and Parts, Biomedical Raw Materials, Industrial Parts, and Metrology Sciences. OPM was selected to participate in the National Additive Manufacturing Innovation Institute (NAMII) in 2012. OPM is certified ISO 13485 and ISO 9001.

For more information, please visit http://www.oxfordpm.com

Read the full story at http://www.prweb.com/releases/2013/02OPM1st510kapproval/prweb10429061.htm.


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