Last synced on 14 November 2025 at 11:06 pm

PROVEN KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K000113
510(k) Type
Traditional
Applicant
STELKAST COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2000
Days to Decision
81 days
Submission Type
Statement

PROVEN KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K000113
510(k) Type
Traditional
Applicant
STELKAST COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2000
Days to Decision
81 days
Submission Type
Statement