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PERIPHERAL AVE STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983008
510(k) Type
Traditional
Applicant
PERIPHERAL AVE
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
11/25/1998
Days to Decision
89 days
Submission Type
Summary

PERIPHERAL AVE STENT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983008
510(k) Type
Traditional
Applicant
PERIPHERAL AVE
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
11/25/1998
Days to Decision
89 days
Submission Type
Summary