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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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Proficient® Posterior Cervical Spine System - 10840642121179

Double Offset Connector, 3.5/4.0(U), 4.0 mm Rod × 21 mm
Spine Wave, Inc.
11-9227
In Commercial Distribution

  • 10840642121179 ()
11-9227

  • Bone-screw internal spinal fixation system connector

Proficient® Posterior Cervical Spine System - 10840642121162

Double Offset Connector, 3.5/4.0(C), 4.0 mm Rod × 21 mm
Spine Wave, Inc.
11-9226
In Commercial Distribution

  • 10840642121162 ()
11-9226

  • Bone-screw internal spinal fixation system connector

Paramount™ Anterior Cervical Spine System - 10840642121025

Lordotic Scoring Trial, 10 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5628
In Commercial Distribution

  • 10840642121025 ()
10-5628

  • Polymeric spinal interbody fusion cage

Paramount™ Anterior Cervical Spine System - 10840642121018

Lordotic Scoring Trial, 9 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5627
In Commercial Distribution

  • 10840642121018 ()
10-5627

  • Polymeric spinal interbody fusion cage

Paramount™ Anterior Cervical Spine System - 10840642121001

Lordotic Scoring Trial, 8 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5626
In Commercial Distribution

  • 10840642121001 ()
10-5626

  • Polymeric spinal interbody fusion cage

Paramount™ Anterior Cervical Spine System - 10840642120998

Lordotic Scoring Trial, 7 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5625
In Commercial Distribution

  • 10840642120998 ()
10-5625

  • Polymeric spinal interbody fusion cage

Paramount™ Anterior Cervical Spine System - 10840642120981

Lordotic Scoring Trial, 6 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5624
In Commercial Distribution

  • 10840642120981 ()
10-5624

  • Polymeric spinal interbody fusion cage

Paramount™ Anterior Cervical Spine System - 10840642120974

Lordotic Scoring Trial, 5 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5623
In Commercial Distribution

  • 10840642120974 ()
10-5623

  • Polymeric spinal interbody fusion cage

Paramount™ Anterior Cervical Spine System - 10840642120967

Lordotic Scoring Trial, 10 mm x 15.5 mm x 14 mm
Spine Wave, Inc.
10-5614
In Commercial Distribution

  • 10840642120967 ()
10-5614

  • Polymeric spinal interbody fusion cage

Paramount™ Anterior Cervical Spine System - 10840642120950

Lordotic Scoring Trial, 9 mm x 15.5 mm x 14 mm
Spine Wave, Inc.
10-5613
In Commercial Distribution

  • 10840642120950 ()
10-5613

  • Polymeric spinal interbody fusion cage
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