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ORTHOMET TITANIUM HYBRID FEMORAL STEM

Page Type
Cleared 510(K)
510(k) Number
K945783
510(k) Type
Traditional
Applicant
ORTHOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/1995
Days to Decision
186 days
Submission Type
Summary

ORTHOMET TITANIUM HYBRID FEMORAL STEM

Page Type
Cleared 510(K)
510(k) Number
K945783
510(k) Type
Traditional
Applicant
ORTHOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/1995
Days to Decision
186 days
Submission Type
Summary