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ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932911
510(k) Type
Traditional
Applicant
DOW CORNING WRIGHT
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
6/30/1994
Days to Decision
379 days
Submission Type
Summary

ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932911
510(k) Type
Traditional
Applicant
DOW CORNING WRIGHT
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
6/30/1994
Days to Decision
379 days
Submission Type
Summary