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ENDURE IMPLANT, MODEL 5108, 5111, 5113, 5114

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072660
510(k) Type
Traditional
Applicant
IMTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/2007
Days to Decision
82 days
Submission Type
Statement

ENDURE IMPLANT, MODEL 5108, 5111, 5113, 5114

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072660
510(k) Type
Traditional
Applicant
IMTEC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/2007
Days to Decision
82 days
Submission Type
Statement