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INTERPORE CROSS INTERNATIONAL ANTERIOR FIXATION DEVICE (AFD)

Page Type
Cleared 510(K)
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)
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