FDA 510(k) Applications Submitted by OSSACUR AG

FDA 510(k) Number Submission Date Device Name Applicant
K050416 02/18/2005 OSSAPLAST ORTHO OSSACUR AG
K051047 04/25/2005 COLLOSS E BONE VOID FILLER OSSACUR AG
K042305 08/25/2004 OSSAPLAST ORTHO, O.5ML, MODEL# 221 900, OSSAPLAST ORTHO, 1.0ML, MODEL# 221 901, OSSAPLAST ORTHO, 3.0ML, MODEL# 221 903 OSSACUR AG
K053374 12/05/2005 OSSAPLAST DENTAL (PARTICLE SIZE OF 500 TO 1000 UM TO 2000 UM) OSSACUR AG


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