Last synced on 2 May 2025 at 11:05 pm

Spine Guidance Software (version 5.0); Xia 3/ Serrato Q Instruments; Everest Q Instruments; Mesa 2 Q Instruments; Q Pedicle Preparation Instruments; Q S2AI Drills; Q Handles; Consolidated Operating Room Equipment (CORE) 2 Console; Electric System 6 Dual Trigger Rotary Handpiece

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240662
510(k) Type
Traditional
Applicant
Stryker Leibinger GmbH & Co. KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/6/2024
Days to Decision
90 days
Submission Type
Summary

Spine Guidance Software (version 5.0); Xia 3/ Serrato Q Instruments; Everest Q Instruments; Mesa 2 Q Instruments; Q Pedicle Preparation Instruments; Q S2AI Drills; Q Handles; Consolidated Operating Room Equipment (CORE) 2 Console; Electric System 6 Dual Trigger Rotary Handpiece

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240662
510(k) Type
Traditional
Applicant
Stryker Leibinger GmbH & Co. KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/6/2024
Days to Decision
90 days
Submission Type
Summary