FDA 510(k) Application Details - K920508

Device Classification Name Bone Grafting Material, Synthetic

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510(K) Number K920508
Device Name Bone Grafting Material, Synthetic
Applicant GEISTLICH-PHARMA
1050 CONNECTICUT AVE. N.W.
WASHINGTON, DC US
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Contact PETER S REICHERTZ
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Regulation Number 872.3930

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Classification Product Code LYC
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Date Received 02/05/1992
Decision Date 11/24/1992
Decision SE - Substantially Equivalent
Classification Advisory Committee DE - Dental
Review Advisory Committee DE - Dental
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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