Last synced on 14 November 2025 at 11:06 pm

primaLOK™ SP Interspinous Fusion System

Page Type
Cleared 510(K)
510(k) Number
K231807
510(k) Type
Traditional
Applicant
Wenzel Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2023
Days to Decision
56 days
Submission Type
Summary

primaLOK™ SP Interspinous Fusion System

Page Type
Cleared 510(K)
510(k) Number
K231807
510(k) Type
Traditional
Applicant
Wenzel Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2023
Days to Decision
56 days
Submission Type
Summary