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ORTELIUS 800

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011827
510(k) Type
Traditional
Applicant
ORTHOSCAN LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/28/2001
Days to Decision
77 days
Submission Type
Summary

ORTELIUS 800

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011827
510(k) Type
Traditional
Applicant
ORTHOSCAN LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/28/2001
Days to Decision
77 days
Submission Type
Summary