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GII SPINAL FIXATION SYSTEM, GII-TI-POLY AXIAL SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083567
510(k) Type
Special
Applicant
CO-LIGNE AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2009
Days to Decision
285 days
Submission Type
Summary

GII SPINAL FIXATION SYSTEM, GII-TI-POLY AXIAL SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083567
510(k) Type
Special
Applicant
CO-LIGNE AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/2009
Days to Decision
285 days
Submission Type
Summary