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MODIFICATION TO ASNIS III CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K024060
510(k) Type
Special
Applicant
HOWMEDICA OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2002
Days to Decision
11 days
Submission Type
Summary

MODIFICATION TO ASNIS III CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K024060
510(k) Type
Special
Applicant
HOWMEDICA OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2002
Days to Decision
11 days
Submission Type
Summary