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FDA 510(k) Applications Submitted by KATHRYN A 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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