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MODIFICATION TO:MICROFUSE BONE VOID FILLER

Page Type
Cleared 510(K)
510(k) Number
K083232
510(k) Type
Traditional
Applicant
GLOBUS MEDICAL INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/24/2008
Days to Decision
51 days
Submission Type
Summary

MODIFICATION TO:MICROFUSE BONE VOID FILLER

Page Type
Cleared 510(K)
510(k) Number
K083232
510(k) Type
Traditional
Applicant
GLOBUS MEDICAL INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/24/2008
Days to Decision
51 days
Submission Type
Summary