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ORTHO ANCHOR SCREWS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073461
510(k) Type
Traditional
Applicant
M.I.S. IMPLANTS TECHNOLOGIES LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
1/25/2008
Days to Decision
46 days
Submission Type
Summary

ORTHO ANCHOR SCREWS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073461
510(k) Type
Traditional
Applicant
M.I.S. IMPLANTS TECHNOLOGIES LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
1/25/2008
Days to Decision
46 days
Submission Type
Summary