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LOWTOP PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K070933
510(k) Type
Traditional
Applicant
SANACOR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2007
Days to Decision
71 days
Submission Type
Summary

LOWTOP PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K070933
510(k) Type
Traditional
Applicant
SANACOR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2007
Days to Decision
71 days
Submission Type
Summary