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REGENEROSS ALLOGRAFT PLUS MINERLIZED

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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