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FIXION INTERLOCKING PROXIMAL FEMORAL NAILING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010988
510(k) Type
Traditional
Applicant
Disc-O-Tech Medical Technologies, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2001
Days to Decision
78 days
Submission Type
Summary

FIXION INTERLOCKING PROXIMAL FEMORAL NAILING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010988
510(k) Type
Traditional
Applicant
Disc-O-Tech Medical Technologies, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/2001
Days to Decision
78 days
Submission Type
Summary