510(k) K242361 · KWQ Appliance, Fixation, Spinal Intervertebral Body
OZARK Cervical Plate System; PYRENEES® Cervical Plate System; EVEREST® Spinal System; MESA® Spinal System; MESA® Small Stature Spinal System; CASPIAN® Spinal System; DENALI® Spinal System; DENALI® MI Spinal System; YUKON OCT Spinal System; Xia® 3 Spinal System; K2M Patient Specific; CASCADIA Interb
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Nov 7, 2024 |
| Received | Aug 9, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242361
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.