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AVERSION PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133103
510(k) Type
Traditional
Applicant
K7 LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2014
Days to Decision
119 days
Submission Type
Summary

AVERSION PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133103
510(k) Type
Traditional
Applicant
K7 LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2014
Days to Decision
119 days
Submission Type
Summary