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SUTURTEK FASTCLOSE STERNUM CLOSURE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032468
510(k) Type
Traditional
Applicant
SUTURTEK INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2003
Days to Decision
43 days
Submission Type
Summary

SUTURTEK FASTCLOSE STERNUM CLOSURE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032468
510(k) Type
Traditional
Applicant
SUTURTEK INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2003
Days to Decision
43 days
Submission Type
Summary