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FDA 510(k) Applications Submitted by OSTEOGENICS CO.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K972278
06/18/1997
CYTOPLAST REGENTEX TITANIUM 250
OSTEOGENICS CO.
K964342
10/31/1996
CYTOPLAST GBR
OSTEOGENICS CO.
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