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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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