K-number	K121183
Device name	COMPREHENSIVE REVERSE SHOULDER - E1 POLYETHYLENE CLAIMS
Applicant	Biomet Corporation
Product code	PHX
Device class	Class II
Decision date	Jul 26, 2012
Decision	Substantially Equivalent
Regulation	888.3660

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View the full FDA submission: accessdata.fda.gov

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COMPREHENSIVE REVERSE SHOULDER - E1 POLYETHYLENE CLAIMS

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