K-number	K150064
Device name	Synthetic Bone Graft (TriPore HA, TriPore BP90, TriPore BP15)
Applicant	Orthogem, Ltd.
Product code	MQV
Device class	Class II
Decision date	Sep 4, 2015
Decision	Substantially Equivalent
Regulation	888.3045

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View the full FDA submission: accessdata.fda.gov

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Synthetic Bone Graft (TriPore HA, TriPore BP90, TriPore BP15)

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