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MODIFICATION TO LIFESTENT SDS AND XL SDS BILIARY ENDOPROSTHESIS

Page Type
Cleared 510(K)
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)
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