Stryker received FDA 510(k) clearance for its OptaBlate system, and Medtronic received clearance for OsteoCool 2.0.
2 reports, 1 independent
Updated Jul 18
Gone quiet
- Reports
- 2
- Developments
- 1
- Repetition
- 50%
New informationRepeats or wire copies
AI-generated analysis. Brind wrote this summary from the reports listed below. It can be wrong. Each section says how much you can rely on it, and the sources are linked so you can check.
What happened
Stryker received FDA 510(k) clearance for its OptaBlate system, and Medtronic received clearance for OsteoCool 2.0.
Who's involved
What this event is mainly aboutKeep exploring
The entities involved
- FDA
-
Stryker Corporation
American medical technologies company
-
Medtronic plc
medical device company
Related events
Coverage
Newest first; wire copies grouped- GlobeNewswireTumor Ablation Market Research Report 2025-2032 | Radiofrequency Ablation Leads, Offering Efficiency and Specificity Across Key Organ Treatments The global tumor ablation market is projected to surge
- Unknown outlet