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MEDTRONIC MIDA REX LEGEND SYSTEM, MIDAS REX LEGEND PNEUMATIC HIGH SPEED SYSTEM OR LEGEND SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020069
510(k) Type
Traditional
Applicant
Medtronic Midas Rex
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/2002
Days to Decision
68 days
Submission Type
Summary

MEDTRONIC MIDA REX LEGEND SYSTEM, MIDAS REX LEGEND PNEUMATIC HIGH SPEED SYSTEM OR LEGEND SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020069
510(k) Type
Traditional
Applicant
Medtronic Midas Rex
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/2002
Days to Decision
68 days
Submission Type
Summary