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MODIFICATION TO: LIGAFIX INTERFERENCE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070507
510(k) Type
Special
Applicant
Science For Biomaterials
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/29/2007
Days to Decision
36 days
Submission Type
Summary

MODIFICATION TO: LIGAFIX INTERFERENCE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070507
510(k) Type
Special
Applicant
Science For Biomaterials
Country
France
FDA Decision
Substantially Equivalent
Decision Date
3/29/2007
Days to Decision
36 days
Submission Type
Summary