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REVLOK FENESTRATED SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110280
510(k) Type
Special
Applicant
GLOBUS MEDICAL INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
7/6/2011
Days to Decision
156 days
Submission Type
Summary

REVLOK FENESTRATED SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110280
510(k) Type
Special
Applicant
GLOBUS MEDICAL INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
7/6/2011
Days to Decision
156 days
Submission Type
Summary