Last synced on 18 April 2025 at 11:05 pm

STELKAST PROVEN KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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