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PATHFINDER NXT MINIMALLY INVASIVE PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K132884
510(k) Type
Traditional
Applicant
ZIMMER SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2013
Days to Decision
73 days
Submission Type
Summary

PATHFINDER NXT MINIMALLY INVASIVE PEDICLE SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K132884
510(k) Type
Traditional
Applicant
ZIMMER SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2013
Days to Decision
73 days
Submission Type
Summary