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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® PEEK IBF System - 00191083032382

TRIAL SPACER
Pioneer Surgical Technology, Inc.
35-DTRL18-13
Not in Commercial Distribution


  • 18mm X 13mm
35-DTRL18-13

  • Surgical implant template, reusable

Cross-Fuse® PEEK IBF System - 00191083032368

TRIAL SPACER
Pioneer Surgical Technology, Inc.
35-DTRL18-11
Not in Commercial Distribution


  • 18mm X 11mm
35-DTRL18-11

  • Surgical implant template, reusable

Cross-Fuse® PEEK IBF System - 00191083032344

TRIAL SPACER
Pioneer Surgical Technology, Inc.
35-DTRL14-9
Not in Commercial Distribution


  • 14mm X 9mm
35-DTRL14-9

  • Surgical implant template, reusable

Cross-Fuse® PEEK IBF System - 00191083032313

TRIAL SPACER
Pioneer Surgical Technology, Inc.
35-DTRL14-15
Not in Commercial Distribution


  • 14mm X 15mm
35-DTRL14-15

  • Surgical implant template, reusable

Cross-Fuse® PEEK IBF System - 00191083032290

TRIAL SPACER
Pioneer Surgical Technology, Inc.
35-DTRL14-13
Not in Commercial Distribution


  • 14mm X 13mm
35-DTRL14-13

  • Surgical implant template, reusable

Cross-Fuse® PEEK IBF System - 00191083032276

TRIAL SPACER
Pioneer Surgical Technology, Inc.
35-DTRL14-11
Not in Commercial Distribution


  • 14mm X 11mm
35-DTRL14-11

  • Surgical implant template, 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
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