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FUSIONSYNC, CHIMAERA FUSIONSYNC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132963
510(k) Type
Traditional
Applicant
CHIMAERA GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/16/2013
Days to Decision
87 days
Submission Type
Summary

FUSIONSYNC, CHIMAERA FUSIONSYNC

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132963
510(k) Type
Traditional
Applicant
CHIMAERA GMBH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/16/2013
Days to Decision
87 days
Submission Type
Summary