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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Bone Grafting Material, Synthetic
510(k) Number K930115
Device Name PERIOGLASS
Applicant
Usbiomaterials Corp.
One Progress Blvd.
Alachua,  FL  32615
Applicant Contact DAVID C GREENSPAN
Correspondent
Usbiomaterials Corp.
One Progress Blvd.
Alachua,  FL  32615
Correspondent Contact DAVID C GREENSPAN
Regulation Number872.3930
Classification Product Code
LYC  
Date Received01/11/1993
Decision Date 11/04/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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