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STELKAST PROVEN KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K002281
510(k) Type
Special
Applicant
STELKAST COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2000
Days to Decision
24 days
Submission Type
Statement

STELKAST PROVEN KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K002281
510(k) Type
Special
Applicant
STELKAST COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2000
Days to Decision
24 days
Submission Type
Statement