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ORTHO ANCHOR SCREWS

Page Type
Cleared 510(K)
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)
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