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OSTEONICS NORMALIZED AD-HA ACETABULAR COMPONENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K970394
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1997
Days to Decision
78 days
Submission Type
Summary

OSTEONICS NORMALIZED AD-HA ACETABULAR COMPONENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K970394
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1997
Days to Decision
78 days
Submission Type
Summary