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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, Animal Source
510(k) Number K122894
FOIA Releasable 510(k) K122894
Device Name GEISTLICH BIO-OSS, GEISTLICH BIO-OSS COLLAGEN, GEISTLICH COMBI-KIT COLLAGEN, GEISTLICH PERIO SYSTEM COMBI PACK, GEISTLIC
Applicant
Geistlich Pharma AG
555 Twelfth St., NW
Washington,  DC  20004 -1206
Applicant Contact DANIEL A KRACOV
Correspondent
Geistlich Pharma AG
555 Twelfth St., NW
Washington,  DC  20004 -1206
Correspondent Contact DANIEL A KRACOV
Regulation Number872.3930
Classification Product Code
NPM  
Date Received09/20/2012
Decision Date 02/15/2013
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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