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OSTEONICS NORMALIZED AD ACETABULAR COMPONENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K970697
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/1997
Days to Decision
58 days
Submission Type
Summary

OSTEONICS NORMALIZED AD ACETABULAR COMPONENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K970697
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/1997
Days to Decision
58 days
Submission Type
Summary