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COMPRESS SEGMENTAL HUMERAL REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K123297
510(k) Type
Special
Applicant
BIOMET MANUFACTUTING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2012
Days to Decision
29 days
Submission Type
Summary

COMPRESS SEGMENTAL HUMERAL REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K123297
510(k) Type
Special
Applicant
BIOMET MANUFACTUTING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2012
Days to Decision
29 days
Submission Type
Summary