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IFS CANNULATED BONE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061620
510(k) Type
Traditional
Applicant
Internal Fixation Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2006
Days to Decision
47 days
Submission Type
Summary

IFS CANNULATED BONE SCREW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061620
510(k) Type
Traditional
Applicant
Internal Fixation Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2006
Days to Decision
47 days
Submission Type
Summary