K-number	K212933
Device name	INHANCETM Hybrid Anatomic Glenoid Implant
Applicant	Depuy Ireland UC
Product code	MBF
Device class	Class II
Decision date	Jun 8, 2022
Decision	Substantially Equivalent
Regulation	888.3670

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Source

View the full FDA submission: accessdata.fda.gov

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INHANCETM Hybrid Anatomic Glenoid Implant

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