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ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMP

Page Type
Cleared 510(K)
510(k) Number
K930189
510(k) Type
Traditional
Applicant
DOW CORNING WRIGHT
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/6/1993
Days to Decision
204 days
Submission Type
Summary

ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMP

Page Type
Cleared 510(K)
510(k) Number
K930189
510(k) Type
Traditional
Applicant
DOW CORNING WRIGHT
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/6/1993
Days to Decision
204 days
Submission Type
Summary