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MODIFICATION AXIOM TOTAL KNEE SYST, PATELLAR COMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912266
510(k) Type
Traditional
Applicant
OROTHMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/20/1991
Days to Decision
90 days
Submission Type
Statement

MODIFICATION AXIOM TOTAL KNEE SYST, PATELLAR COMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912266
510(k) Type
Traditional
Applicant
OROTHMET, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
8/20/1991
Days to Decision
90 days
Submission Type
Statement