K-number	K222363
Device name	Aevumed PHANTOM-LP Suture Anchors
Applicant	Aevumed, Inc.
Product code	MBI
Device class	Class II
Decision date	Nov 28, 2022
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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Aevumed PHANTOM-LP Suture Anchors

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Aevumed PHANTOM-LP Suture Anchors