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ANNULOFLEX ANNULOPLASTY SYSTEM, MODEL AF800

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992056
510(k) Type
Traditional
Applicant
Sulzer Carbomedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/1999
Days to Decision
116 days
Submission Type
Summary

ANNULOFLEX ANNULOPLASTY SYSTEM, MODEL AF800

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992056
510(k) Type
Traditional
Applicant
Sulzer Carbomedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/12/1999
Days to Decision
116 days
Submission Type
Summary