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LIFESTENT SDS BILIARY ENDOPROSTHESIS, LIFESTENT XL SDS BILIARY ENDOPROSTHESIS

Page Type
Cleared 510(K)
510(k) Number
K023308
510(k) Type
Traditional
Applicant
ORBUS MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
4/14/2003
Days to Decision
193 days
Submission Type
Summary

LIFESTENT SDS BILIARY ENDOPROSTHESIS, LIFESTENT XL SDS BILIARY ENDOPROSTHESIS

Page Type
Cleared 510(K)
510(k) Number
K023308
510(k) Type
Traditional
Applicant
ORBUS MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
4/14/2003
Days to Decision
193 days
Submission Type
Summary