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AXIOM TOTAL KNEE SYST/ACL RETAIN TIBIAL TRAY/INSER

Page Type
Cleared 510(K)
510(k) Number
K926334
510(k) Type
Traditional
Applicant
ORTHOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/18/1994
Days to Decision
671 days
Submission Type
Summary

AXIOM TOTAL KNEE SYST/ACL RETAIN TIBIAL TRAY/INSER

Page Type
Cleared 510(K)
510(k) Number
K926334
510(k) Type
Traditional
Applicant
ORTHOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
10/18/1994
Days to Decision
671 days
Submission Type
Summary