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REGENEROSS ALLOGRAFT PLUS MINERLIZED

Page Type
Cleared 510(K)
510(k) Number
K113645
510(k) Type
Special
Applicant
BIOMET INTERPORE CROSS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2012
Days to Decision
39 days
Submission Type
Summary

REGENEROSS ALLOGRAFT PLUS MINERLIZED

Page Type
Cleared 510(K)
510(k) Number
K113645
510(k) Type
Special
Applicant
BIOMET INTERPORE CROSS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2012
Days to Decision
39 days
Submission Type
Summary