Last synced on 14 November 2025 at 11:06 pm

POSTERIOR ANNULOPLASTY BAND (MODEL 607)

Page Type
Cleared 510(K)
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)
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