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INTRASTENT DOUBLESTRUT LD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993904
510(k) Type
Traditional
Applicant
INTRATHERAPEUTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
2/1/2000
Days to Decision
76 days
Submission Type
Summary

INTRASTENT DOUBLESTRUT LD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993904
510(k) Type
Traditional
Applicant
INTRATHERAPEUTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
2/1/2000
Days to Decision
76 days
Submission Type
Summary