Last synced on 2 May 2025 at 11:05 pm

Spine Guidance Software (Version 5.1); Consolidated Operating Room Equipment (CORE) 2 Console; CORE Q Footswitch; PI Drive 2 Motors; Elite Q Attachments and Cutting Accessories

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241171
510(k) Type
Traditional
Applicant
Stryker Leibinger GmbH & Co. KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
7/25/2024
Days to Decision
90 days
Submission Type
Summary

Spine Guidance Software (Version 5.1); Consolidated Operating Room Equipment (CORE) 2 Console; CORE Q Footswitch; PI Drive 2 Motors; Elite Q Attachments and Cutting Accessories

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241171
510(k) Type
Traditional
Applicant
Stryker Leibinger GmbH & Co. KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
7/25/2024
Days to Decision
90 days
Submission Type
Summary