Catalyst
Slingshot members are tracking this event:
Stryker receives FDA 510(k) clearance for its Tritanium PL Posterior Lumbar Cage for use in spinal fixation in patients with degenerative disc disease
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Related Companies | Importance
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Impact on Stocks
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SYK | Community voting in process |
Additional Information
Slingshot Insights Explained
Catalyst Date
Occurred on:
Mar 04, 2016
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Related Keywords
Tritanium Pl Posterior Lumbar Cage, Spinal Fixation, Degenerative Disc Disease, Porous Titanium Material