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COMPRESS SEGMENTAL HUMERAL REPLACEMENT SYSTEM

Biomet Manufactuting Corp. · Class II · Cleared Nov 20, 2012

K-numberK123297
Device nameCOMPRESS SEGMENTAL HUMERAL REPLACEMENT SYSTEM
ApplicantBiomet Manufactuting Corp.
Product codeMBF
Device classClass II
Decision dateNov 20, 2012
DecisionSubstantially Equivalent
Regulation888.3670
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View the full FDA submission: accessdata.fda.gov

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