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subpart-f—cardiovascular-therapeutic-devices/

SPRINTER LEGEND 1.25MM RX AND SPRINTER LEGEND 1.25MM OTW BALLOON

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K103095
510(k) Type: Traditional
Applicant: MEDTRONIC IRELAND
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 10/22/2010
Days to Decision: 14 days
Submission Type: Summary

FDA Browser

subpart-f—cardiovascular-therapeutic-devices/

SPRINTER LEGEND 1.25MM RX AND SPRINTER LEGEND 1.25MM OTW BALLOON

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K103095
510(k) Type: Traditional
Applicant: MEDTRONIC IRELAND
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 10/22/2010
Days to Decision: 14 days
Submission Type: Summary