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MG II POROUS KNEE SYSTEM FEMORAL COMPONENTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930831
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1993
Days to Decision
272 days
Submission Type
Statement

MG II POROUS KNEE SYSTEM FEMORAL COMPONENTS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930831
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1993
Days to Decision
272 days
Submission Type
Statement