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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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Cross-Fuse® II PEEK IBF System - 00191083041032

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-1435-15
In Commercial Distribution


  • 14mm (W) x 15mm (H) x 35mm (L)
38-1435-15

  • Polymeric spinal interbody fusion cage

Cross-Fuse® II PEEK IBF System - 00191083041018

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


  • 14mm (W) x 11mm (H) x 35mm (L)
38-1435-11

  • Polymeric spinal interbody fusion cage

Cross-Fuse® PEEK IBF System - 00191083033686

INSTRUMENT CASE
Pioneer Surgical Technology, Inc.
35-CASE
Not in Commercial Distribution

  • 00191083033686 ()
35-CASE

  • Device sterilization/disinfection container, reusable

Cross-Fuse® II PEEK IBF System - 00191083033358

TAMP
Rti Surgical, Inc.
38-TAMP
In Commercial Distribution

38-TAMP

  • Surgical tamp, reusable

Cross-Fuse® II PEEK IBF System - 00191083032269

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2670-9-6L
In Commercial Distribution

  • 00191083032269 ()

  • 26mm (W) x 9mm (H) x 70mm (L) x 6 Degrees Lordosis
38-2670-9-6L

  • Polymeric spinal interbody fusion cage

Cross-Fuse® II PEEK IBF System - 00191083032245

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2670-17-12L
In Commercial Distribution

  • 00191083032245 ()

  • 26mm (W) x 17mm (H) x 70mm (L) x 12 Degrees Lordosis
38-2670-17-12L

  • Polymeric spinal interbody fusion cage

Cross-Fuse® II PEEK IBF System - 00191083032221

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2670-15-12L
In Commercial Distribution

  • 00191083032221 ()

  • 26mm (W) x 15mm (H) x 70mm (L) x 12 Degrees Lordosis
38-2670-15-12L

  • Polymeric spinal interbody fusion cage

Cross-Fuse® II PEEK IBF System - 00191083032207

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2670-13-12L
In Commercial Distribution

  • 00191083032207 ()

  • 26mm (W) x 13mm (H) x 70mm (L) x 12 Degrees Lordosis
38-2670-13-12L

  • Polymeric spinal interbody fusion cage

Cross-Fuse® II PEEK IBF System - 00191083032184

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2670-11-12L
In Commercial Distribution

  • 00191083032184 ()

  • 26mm (W) x 11mm (H) x 70mm (L) x 12 Degrees Lordosis
38-2670-11-12L

  • Polymeric spinal interbody fusion cage

Cross-Fuse® II PEEK IBF System - 00191083032177

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2665-9-6L
In Commercial Distribution

  • 00191083032177 ()

  • 26mm (W) x 9mm (H) x 65mm (L) x 6 Degrees Lordosis
38-2665-9-6L

  • Polymeric spinal interbody fusion cage
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