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POSTERIOR ANNULOPLASTY BAND (MODEL 607)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960356
510(k) Type
Traditional
Applicant
THE HEART VALVE DIV. MEDTRONIC CARDIOVASCULAR SURG
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
8/27/1996
Days to Decision
215 days

POSTERIOR ANNULOPLASTY BAND (MODEL 607)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960356
510(k) Type
Traditional
Applicant
THE HEART VALVE DIV. MEDTRONIC CARDIOVASCULAR SURG
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
8/27/1996
Days to Decision
215 days