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ASNIS III CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K000080
510(k) Type
Traditional
Applicant
HOWMEDICA OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2000
Days to Decision
83 days
Submission Type
Summary

ASNIS III CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K000080
510(k) Type
Traditional
Applicant
HOWMEDICA OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2000
Days to Decision
83 days
Submission Type
Summary