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TRANSET FRACTURE FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033717
510(k) Type
Traditional
Applicant
Bonutti Research, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2004
Days to Decision
91 days
Submission Type
Summary

TRANSET FRACTURE FIXATION SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033717
510(k) Type
Traditional
Applicant
Bonutti Research, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2004
Days to Decision
91 days
Submission Type
Summary