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PROVEN REVISION MODULAR TIBIAL TRAY

Page Type
Cleared 510(K)
510(k) Number
K051976
510(k) Type
Traditional
Applicant
STELKAST COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2005
Days to Decision
88 days
Submission Type
Statement

PROVEN REVISION MODULAR TIBIAL TRAY

Page Type
Cleared 510(K)
510(k) Number
K051976
510(k) Type
Traditional
Applicant
STELKAST COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2005
Days to Decision
88 days
Submission Type
Statement