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INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022143
510(k) Type
Traditional
Applicant
INTERPORE CROSS INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2003
Days to Decision
205 days
Submission Type
Summary

INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022143
510(k) Type
Traditional
Applicant
INTERPORE CROSS INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2003
Days to Decision
205 days
Submission Type
Summary