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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Filler, Bone Void, Calcium Compound
510(k) Number K041889
FOIA Releasable 510(k) K041889
Device Name TRI-OSTETIC
Applicant
Berkeley Advanced Biomaterials, Inc.
1933 Davis St. Suite 307
San Leandro,  CA  94577
Applicant Contact FRANCOIS GENIN
Correspondent
Berkeley Advanced Biomaterials, Inc.
1933 Davis St. Suite 307
San Leandro,  CA  94577
Correspondent Contact FRANCOIS GENIN
Regulation Number888.3045
Classification Product Code
MQV  
Date Received07/12/2004
Decision Date 08/19/2004
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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