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MODIFICATION TO FIXION INTERLOCKING INTRAMEDULLARY NAILING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013449
510(k) Type
Traditional
Applicant
DISC-O-TECH MEDICAL TECHNOLOGIES, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/19/2001
Days to Decision
63 days
Submission Type
Summary

MODIFICATION TO FIXION INTERLOCKING INTRAMEDULLARY NAILING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013449
510(k) Type
Traditional
Applicant
DISC-O-TECH MEDICAL TECHNOLOGIES, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/19/2001
Days to Decision
63 days
Submission Type
Summary