FDA 510(k) Applications Submitted by U.S. BIOMATERIALS CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K000149 01/19/2000 NOVABONE-BIOGLASS BONE GRAFT PARTICULATE U.S. BIOMATERIALS CORP.
K992416 07/20/1999 PERIOGLAS- BIOGLASS BONE GRAFT PARTICULATE U.S. BIOMATERIALS CORP.
K962494 06/26/1996 PERIOGLAS - BIOGLASS BONE GRAFT PARTICULATE U.S. BIOMATERIALS CORP.


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