FDA 510(k) Applications Submitted by HDC S.R.L.

FDA 510(k) Number Submission Date Device Name Applicant
K091390 05/11/2009 HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2 HDC S.R.L.
K071851 07/05/2007 HDC STERILE SPIDER SCREW HDC S.R.L.
K052471 09/08/2005 HDC SPIDER SCREW HDC S.R.L.


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