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BALANCED KNEE SYSTEM MODULAR REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K060569
510(k) Type
Traditional
Applicant
ORTHO DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2006
Days to Decision
125 days
Submission Type
Statement

BALANCED KNEE SYSTEM MODULAR REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K060569
510(k) Type
Traditional
Applicant
ORTHO DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2006
Days to Decision
125 days
Submission Type
Statement