Last synced on 2 December 2022 at 11:04 pm

MODIFICATION TO LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041032
510(k) Type
Special
Applicant
ORBUS MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
5/10/2004
Days to Decision
19 days
Submission Type
Summary

MODIFICATION TO LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K041032
510(k) Type
Special
Applicant
ORBUS MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
5/10/2004
Days to Decision
19 days
Submission Type
Summary