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KMEDIC EXTERNAL FIXATION DEVICES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030336
510(k) Type
Traditional
Applicant
Teleflex Medical Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2003
Days to Decision
34 days
Submission Type
Summary

KMEDIC EXTERNAL FIXATION DEVICES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030336
510(k) Type
Traditional
Applicant
Teleflex Medical Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2003
Days to Decision
34 days
Submission Type
Summary