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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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