SEARCH RESULTS FOR: 得克萨斯A(76830 results)

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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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Spinal Jaxx Interbody Fusion Device - 00818956020047

Spinal Jaxx Implant, 7Hx10Wx29L mm
NEUROPRO SPINAL JAXX INC.
100001-505
In Commercial Distribution

  • 00818956020047 ()

  • Length: 29 Millimeter
  • Width: 10 Millimeter
  • Height: 7 Millimeter
100001-505

  • Polymeric spinal interbody fusion cage
  • Metallic spinal interbody fusion cage

Spinal Jaxx Interbody Fusion Device - 00818956020030

Spinal Jaxx Implant, 7Hx12Wx25L mm
NEUROPRO SPINAL JAXX INC.
100001-504
In Commercial Distribution

  • 00818956020030 ()

  • Height: 7 Millimeter
  • Width: 12 Millimeter
  • Length: 25 Millimeter
100001-504

  • Polymeric spinal interbody fusion cage
  • Metallic spinal interbody fusion cage

Spinal Jaxx Interbody Fusion Device - 00818956020023

Spinal Jaxx Implant, 7Hx10Wx25L mm
NEUROPRO SPINAL JAXX INC.
100001-503
In Commercial Distribution

  • 00818956020023 ()

  • Length: 25 Millimeter
  • Width: 10 Millimeter
  • Height: 7 Millimeter
100001-503

  • Polymeric spinal interbody fusion cage
  • Metallic spinal interbody fusion cage

Spinal Jaxx Interbody Fusion Device - 00818956020016

Spinal Jaxx Implant, 7Hx12Wx21L mm
NEUROPRO SPINAL JAXX INC.
100001-502
In Commercial Distribution

  • 00818956020016 ()

  • Length: 21 Millimeter
  • Width: 12 Millimeter
  • Height: 7 Millimeter
100001-502

  • Polymeric spinal interbody fusion cage
  • Metallic spinal interbody fusion cage

Spinal Jaxx Interbody Fusion Device - 00818956020009

Spinal Jaxx Implant, 7Hx10Wx21L mm
NEUROPRO SPINAL JAXX INC.
100001-501
In Commercial Distribution

  • 00818956020009 ()

  • Height: 7 Millimeter
  • Width: 10 Millimeter
  • Length: 21 Millimeter
100001-501

  • Polymeric spinal interbody fusion cage
  • Metallic spinal interbody fusion cage

Cross-Fuse® II PEEK IBF System - 00191083043265

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2670-7
In Commercial Distribution

  • 00191083043265 ()

  • 26mm (W) x 7mm (H) x 70mm (L)
38-2670-7

  • Polymeric spinal interbody fusion cage

Cross-Fuse® II PEEK IBF System - 00191083042695

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-1435-11-6C
In Commercial Distribution

  • 00191083042695 ()

  • 14mm (W) x 11mm (H) x 35mm (L) x 5 Degrees Coronal
38-1435-11-6C

  • Polymeric spinal interbody fusion cage

Cross-Fuse® II PEEK IBF System - 00191083042688

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2670-17
In Commercial Distribution

  • 00191083042688 ()

  • 26mm (W) x 17mm (H) x 70mm (L)
38-2670-17

  • Polymeric spinal interbody fusion cage

Cross-Fuse® II PEEK IBF System - 00191083042657

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2670-11
In Commercial Distribution

  • 00191083042657 ()

  • 26mm (W) x 11mm (H) x 70mm (L)
38-2670-11

  • Polymeric spinal interbody fusion cage

Cross-Fuse® II PEEK IBF System - 00191083042640

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2665-9
In Commercial Distribution

  • 00191083042640 ()

  • 26mm (W) x 9mm (H) x 65mm (L)
38-2665-9

  • Polymeric spinal interbody fusion cage
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