PRECICE STRYDE SystemRecalls & reported problems across all models
Nuvasive Specialized Orthopedics, Inc. · 231 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
PRECICE STRYDE System models — page 3
231 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- PRECICE® STRYDE System STP4.5-700Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP4.5-750Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP4.5-800Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP5-200Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP5-225Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP5-250Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP5-275Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP5-300Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP5-325Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP5-375Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP5-425Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP5-550Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP5-600Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP5-650Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP5-750Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System STP5-800Screw, Fixation, Bone2 recalls0 reports
- PRECICE® STRYDE System PS10.0-50SJ235Rod, Fixation, Intramedullary And Accessories1 recall12 reports
- PRECICE® STRYDE System PS10.0-65D250Rod, Fixation, Intramedullary And Accessories1 recall10 reports
- PRECICE® STRYDE System PS10.0-50D235Rod, Fixation, Intramedullary And Accessories1 recall7 reports
- PRECICE® STRYDE System PS10.0-80D305Rod, Fixation, Intramedullary And Accessories1 recall4 reports
- PRECICE® STRYDE System PS10.0-50C235Rod, Fixation, Intramedullary And Accessories1 recall1 report
- PRECICE® STRYDE System PS10.0-80A265Rod, Fixation, Intramedullary And Accessories1 recall0 reports
- PRECICE® STRYDE System PS10.0-80A280Rod, Fixation, Intramedullary And Accessories1 recall0 reports
- PRECICE® STRYDE System PS13.0-80A265Rod, Fixation, Intramedullary And Accessories1 recall0 reports
- PRECICE® STRYDE System PS11.5-80C280Rod, Fixation, Intramedullary And Accessories1 recall0 reports
- PRECICE® STRYDE System PS10.0-50E235Rod, Fixation, Intramedullary And Accessories1 recall0 reports
- PRECICE® STRYDE System PS10.0-50V235Rod, Fixation, Intramedullary And Accessories1 recall0 reports
- PRECICE® STRYDE System PS10.0-65X250Rod, Fixation, Intramedullary And Accessories1 recall0 reports
- PRECICE® STRYDE System STP4.5-275Screw, Fixation, Bone1 recall0 reports
- PRECICE® STRYDE System STP5-450Screw, Fixation, Bone1 recall0 reports
- PRECICE® STRYDE System STP5-475Screw, Fixation, Bone1 recall0 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page