FDA.reportPublic FDA data

Device Listing 2057972708

Listing Summary#

Listing key
2057972708
Premarket submission
K241171
Device
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
Applicant
Stryker Leibinger GmbH & Co KG
Product code
OLO
Decision date
2024-07-25