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WBR XPRESS.CARDIAC, WBR XPRESS.BONE; WBR XACT.CARDIAC, WBR XACT.BONE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080784
510(k) Type
Special
Applicant
ULTRASPECT LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/2/2008
Days to Decision
13 days
Submission Type
Summary

WBR XPRESS.CARDIAC, WBR XPRESS.BONE; WBR XACT.CARDIAC, WBR XACT.BONE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080784
510(k) Type
Special
Applicant
ULTRASPECT LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/2/2008
Days to Decision
13 days
Submission Type
Summary