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LIFESTENT LP SDS BILIARY ENDOPROSTHESIS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023248
510(k) Type
Traditional
Applicant
ORBUS MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
2/11/2003
Days to Decision
134 days
Submission Type
Summary

LIFESTENT LP SDS BILIARY ENDOPROSTHESIS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023248
510(k) Type
Traditional
Applicant
ORBUS MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
2/11/2003
Days to Decision
134 days
Submission Type
Summary