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MODIFICATION TO MICROFUSE BONE VOID FILLER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082442
510(k) Type
Special
Applicant
GLOBUS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2008
Days to Decision
43 days
Submission Type
Summary

MODIFICATION TO MICROFUSE BONE VOID FILLER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082442
510(k) Type
Special
Applicant
GLOBUS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2008
Days to Decision
43 days
Submission Type
Summary