Last synced on 14 November 2025 at 11:06 pm

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

Page Type
Cleared 510(K)
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)
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