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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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