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TWINFIX INTERFRAGMENTARY COMPRESSION SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013775
510(k) Type
Special
Applicant
Stryker Leibinger
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2002
Days to Decision
56 days
Submission Type
Summary

TWINFIX INTERFRAGMENTARY COMPRESSION SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013775
510(k) Type
Special
Applicant
Stryker Leibinger
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2002
Days to Decision
56 days
Submission Type
Summary