About Us At Amedica, we have the scientific and manufacturing expertise to produce medical grade silicon nitride - a patented platform technology for use in a variety of medical applications. Silicon nitride is bioactive and compatible across all imaging modalities, offering surgeons and patients a preferable alternative to commonly used materials. We are the only FDA registered and ISO 13485 certified silicon nitride medical device manufacturing facility in the world. 23.72M outstanding http://www.amedica.com/
SALT LAKE CITY, UT--(Marketwired - Oct 6, 2016) - Amedica Corporation ( NASDAQ : AMDA ), a biomaterial company that develops and commercializes silicon nitride for biomedical applications, today provided a business update related to its business strategy and certain recent developments. Briefly, the updates relate to the following items: New patent directed to a threaded design in ceramic implants; Participation at the annual International Society for Technology in Arthroplasty; and Update related to completion of the company's strategic workforce reducti
Thanks for your help Gil. I was going to add more info. Waiting on a reply from the company about this weeks presentation to see if they can send me something to share.
The Company has a compliance period of 180 calendar days, or until February 13, 2017, to regain compliance with Nasdaq’s minimum bid price requirement. https://www.sec.gov/Archives/edgar/data/1269026/000149315216012693/ex99-1.htm Wanted to make sure I mentioned this.
Device Classification Name orthosis, spinal pedicle fixation, for degenerative disc disease22 510(k) Number K162160 Device Name Preference Elite Pedicle Screw System Applicant AMEDICA CORPORATION 1885 w 2100 s salt lake city, UT 84119 Applicant Contact shanna ryan Correspondent AMEDICA CORPORATION 1885 west 2100 south salt lake city, UT 84119 Correspodent Contact shanna ryan Regulation Number 888.307023 Classification Product Code NKB24 Subsequent Product Codes KWP25 MNH26 MNI27 Date Received 08/02/2016 Decision Date 11/18/2016 Decision substantially equivalent (SESE) Regulation Medical Specialty Orthopedic 510k Review Panel Orthopedic Type Traditional Reviewed by Third Party No Combination Product No https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K162160
