Vimarsana.com

Latest Breaking News On - Da 510k clearance - Page 1 : vimarsana.com

Nevro earns FDA clearance for SI joint fixation system

Nevro earned FDA 510(k) clearance to use its sacroiliac joint fixation system without having to include a lateral screw, the devicemaker said Feb. 28.

Kevin-thornal
Vyrsa-technologies
Meta-keywords-nevro
Da-510k-clearance
Acroiliac-joint-fixation-system
Ateral-screw
Devicemaker
Transfix
Ong-term-fusion
Self-contained
Deployable

Medtech news ASC leaders should know

Discover the latest developments in medtech, including FDA approvals, new appointments, and partnerships that ASC leaders should know about.

Raman-venkatesh
Zimmer-biomet
Medtronic
Waldemar-link-gmbh-co
Momentum-health
Momentum-spine
Bone-ortho
Waldemar-link-gmbh
Medtech
Asc-leaders
Zimmer-biomet
Fda-clearance

Orthofix launches new bioactive synthetic graft

Orthofix earned FDA 510(k) clearance for its OsteoCove advance bioactive synthetic graft, the company said Oct. 12.

Tyler-lipschultz
Orthofix
Da-510k-clearance
Steocove
Ioactive-synthetic-graft
Dputty
Trip-configurations
Hydroxyapatite
Typei-bovine

vimarsana © 2020. All Rights Reserved.