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MG II POROUS KNEE SYSTEM FEMORAL COMPONENTS

Page Type
Cleared 510(K)
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)
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