Last synced on 25 January 2026 at 3:41 am

CRESCO TI IMPLANT CONCEPT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981052
510(k) Type
Traditional
Applicant
Cresco TI Systems AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2001
Days to Decision
1366 days
Submission Type
Statement

CRESCO TI IMPLANT CONCEPT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981052
510(k) Type
Traditional
Applicant
Cresco TI Systems AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2001
Days to Decision
1366 days
Submission Type
Statement