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SUTURTEK 360 DEGREE STERNAL CLOSURE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082828
510(k) Type
Special
Applicant
SUTURTEK INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/2008
Days to Decision
19 days
Submission Type
Summary

SUTURTEK 360 DEGREE STERNAL CLOSURE DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082828
510(k) Type
Special
Applicant
SUTURTEK INCORPORATED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/2008
Days to Decision
19 days
Submission Type
Summary