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ADVENT IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K002614
510(k) Type
Traditional
Applicant
CORE-VENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2000
Days to Decision
108 days
Submission Type
Statement

ADVENT IMPLANT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K002614
510(k) Type
Traditional
Applicant
CORE-VENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/8/2000
Days to Decision
108 days
Submission Type
Statement