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SpineUp Announces U.S. FDA 510(K) Clearance for its New Cervical Cage in Peek HA-Enhanced

March 1, 2022 By SPINEMarketGroup

February 28, 2022– SpineUp a privately held medical technology company has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its brand new cervical cage in Peek Optima HA-Enhanced, Romero.They offer to the surgeons 4 types of cervical cages: Lordotic with screw (self-tapping or self-drilling), anatomic with screw, anatomic and lordotic without fixation.

Romero Cages Features and Benefits:

  • HA-Enhanced Peek for Better Osteointegration
  • Screw Hole Placement Designed Specifically for Surgeon’s Comfort
  • Innovative Self-Tapping & Self-Drilling Set Screw to Better Facilitate Surgeon’s Steps
  • Self-Locking Mechanism for a Quick & Secure Fixation, patented and unique.
  • Large & Wide Range of Sizes & Footprints to Better Address Patients’ Anatomic Variations: 4 to 13mm, 3 Footprints* (*The H04 and H05 height do not exist in 14x12mm footprint)

You will find more information about the implant on https://spineup.tech

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Filed Under: FDA, NEWS Tagged With: 2022, NEWS

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