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SUBCUPASS TUNNELING TOOL

Page Type
Cleared 510(K)
510(k) Number
K780579
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/1978
Days to Decision
39 days

SUBCUPASS TUNNELING TOOL

Page Type
Cleared 510(K)
510(k) Number
K780579
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/1978
Days to Decision
39 days