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IBIS PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K142146
510(k) Type
Traditional
Applicant
ORTHO DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2014
Days to Decision
128 days
Submission Type
Summary

IBIS PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K142146
510(k) Type
Traditional
Applicant
ORTHO DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/2014
Days to Decision
128 days
Submission Type
Summary