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PLACER MODEL 6232 STEERABLE STYLET

Page Type
Cleared 510(K)
510(k) Number
K000955
510(k) Type
Traditional
Applicant
Medtronic Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2000
Days to Decision
84 days
Submission Type
Summary

PLACER MODEL 6232 STEERABLE STYLET

Page Type
Cleared 510(K)
510(k) Number
K000955
510(k) Type
Traditional
Applicant
Medtronic Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2000
Days to Decision
84 days
Submission Type
Summary