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SEPRAMESH, MODEL 5959-1214

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063739
510(k) Type
Traditional
Applicant
GENZYME CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2007
Days to Decision
30 days
Submission Type
Summary

SEPRAMESH, MODEL 5959-1214

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063739
510(k) Type
Traditional
Applicant
GENZYME CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/2007
Days to Decision
30 days
Submission Type
Summary