Last synced on 19 July 2024 at 11:05 pm

ARTELON SURGICAL SUTURE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052482
510(k) Type
Special
Applicant
ARTIMPLANT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2005
Days to Decision
38 days
Submission Type
Summary

ARTELON SURGICAL SUTURE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K052482
510(k) Type
Special
Applicant
ARTIMPLANT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/17/2005
Days to Decision
38 days
Submission Type
Summary