K-number	K171037
Device name	PoreStar Patient Specific Implant
Applicant	Anatomics Pty, Ltd.
Product code	JOF
Device class	Class II
Decision date	Dec 27, 2017
Decision	Substantially Equivalent
Regulation	874.3620

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Source

View the full FDA submission: accessdata.fda.gov

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PoreStar Patient Specific Implant

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