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COMPREHENSIVE REVERSE SHOULDER SCREWS

Page Type
Cleared 510(K)
510(k) Number
K132239
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2013
Days to Decision
50 days
Submission Type
Summary

COMPREHENSIVE REVERSE SHOULDER SCREWS

Page Type
Cleared 510(K)
510(k) Number
K132239
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2013
Days to Decision
50 days
Submission Type
Summary