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OSTEONICS SCORPIO POSTERIOR CRUCIATE RETAINING TOTAL KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K974556
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1998
Days to Decision
84 days
Submission Type
Summary

OSTEONICS SCORPIO POSTERIOR CRUCIATE RETAINING TOTAL KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K974556
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1998
Days to Decision
84 days
Submission Type
Summary