FDA 510(k) Applications Submitted by KATHRYN JAYNE

FDA 510(k) Number Submission Date Device Name Applicant
K161041 04/13/2016 OsteoMed ExtremiLOCK Wrist Plating System OSTEOMED
K121340 05/03/2012 SOMNODENT G2 SOMNOMED INC.
K140278 02/03/2014 SOMNODENT FUSION, CLASSIC; SOMNODENT FUSION, FLEX SOMNOMED INC.
K130558 03/04/2013 SOMNODENT HERBST; CLASSIC, FLEX SOMNOMED INC.
K162542 09/12/2016 OsteoMed PINNACLE Driver OSTEOMED
K162544 09/12/2016 OsteoMed PINNACLE Driver OSTEOMED


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