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Arcuate fixation member

  • US 9,925,056 B2
  • Filed: 03/03/2016
  • Issued: 03/27/2018
  • Est. Priority Date: 04/15/2009
  • Status: Active Grant
First Claim
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1. An intervertebral implant comprising:

  • a spacer body configured to be implanted into an intervertebral space, the spacer body defining an upper bone-engaging surface, a lower bone-engaging surface spaced apart from the upper bone-engaging surface, and an outer wall that extends from the upper bone-engaging surface to the lower bone-engaging surface and defines i) a posterior wall, ii) an anterior wall opposite the posterior wall, and iii) a pair of side walls that extend between the posterior wall and the anterior wall, wherein the side walls are spaced apart from each other along a first direction, the anterior and posterior walls are spaced from each other along a second direction that is perpendicular to the first direction, the outer wall at least partially defines a pair of apertures that each extends along a third direction that is perpendicular to the first and second directions through the upper and lower bone-engaging surfaces at a location between the posterior and anterior walls, the spacer body further includes an inner wall that separates one of the pair of apertures from the other of the pair of apertures with respect to the first direction, the inner wall extends along the second direction substantially from a first direction midpoint of the posterior wall to the anterior wall, the posterior wall defines an inner surface that defines a first cavity that is open to the one of the pair of apertures and a second cavity that is open to the other of the pair of apertures, each of the cavities defines a recessed surface that is positioned intermediate the inner surface and an outer surface of the posterior wall, and each of the cavities extends across a third direction midpoint of the posterior wall; and

    an insert plate configured to be coupled to the spacer body, the insert plate defining at least one guide aperture that extends therethrough and is configured to receive a curved bone fixation member.

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