Last synced on 18 April 2025 at 11:05 pm

ENDURE IMPLANT, MODEL 3508,3511,3514,4308,4311,4314

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030243
510(k) Type
Traditional
Applicant
IMTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2003
Days to Decision
90 days
Submission Type
Statement

ENDURE IMPLANT, MODEL 3508,3511,3514,4308,4311,4314

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030243
510(k) Type
Traditional
Applicant
IMTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/2003
Days to Decision
90 days
Submission Type
Statement