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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 - 00191083030777

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-1860-9-6L
In Commercial Distribution


  • 26mm (W) x 9mm (H) x 60mm (L)
38-1860-9-6L

  • Polymeric spinal interbody fusion cage

Cross-Fuse® II PEEK IBF System - 00191083030760

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-1860-9-12L
In Commercial Distribution


  • 26mm (W) x 15mm (H) x 60mm (L)
38-1860-9-12L

  • Polymeric spinal interbody fusion cage

V. Mueller - 10885403016035

GENESIS STACKING BASKET HALF-LGTH, 9X10 inches22.9X25.4CM 2 inches5.1CM DEEP PERFORATED, ELECTROPOLISHED
STERIS CORPORATION
BP1-2AS
In Commercial Distribution

  • 10885403016035 ()
BP12AS

  • Device sterilization/disinfection container, reusable

Cross-Fuse® II PEEK IBF System - 00191083030746

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-1860-17-18L
In Commercial Distribution


  • 26mm (W) x 17mm (H) x 55mm (L)
38-1860-17-18L

  • Polymeric spinal interbody fusion cage

V. Mueller - 10885403016004

GENESIS STACKING BASKET QTR-LENGTH 9X10 inches22.9X25.4CM 1 inches2.5CM DEEP PERFORATED, ELECTROPOLISHED
STERIS CORPORATION
BP1-1AS
In Commercial Distribution

  • 10885403016004 ()
BP11AS

  • Device sterilization/disinfection container, reusable

V. Mueller - 10885403015991

GENESIS QUARTER-SIZE BASKET 7 X 11 inches 17.8 X 27.9 CM 2 inches 5.1 CM DEEP PERFORATED; VERTICAL HANDLE
STERIS CORPORATION
BP0-2V
In Commercial Distribution

  • 10885403015991 ()
BP02V

  • Device sterilization/disinfection container, reusable

V. Mueller - 10885403015977

GENESIS QTR-LENGTH BASKET 7 X 11 inches17.7 X 27.9CM 2 inches5.1CM DEEP PERFORATED, ELECTROPOLISHED
STERIS CORPORATION
BP0-2A
In Commercial Distribution

  • 10885403015977 ()
BP02A

  • Device sterilization/disinfection container, reusable

Cross-Fuse® II PEEK IBF System - 00191083030715

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-1860-15-18L
In Commercial Distribution


  • 26mm (W) x 17mm (H) x 50mm (L)
38-1860-15-18L

  • Polymeric spinal interbody fusion cage

V. Mueller - 10885403015953

MEDIASTINOSCOPY ASPIRATING NEEDLE 22GA
STERIS CORPORATION
BE8230
In Commercial Distribution

  • 10885403015953 ()
BE8230

  • Surgical/emergency suction cannula, non-illuminating, reusable

Cross-Fuse® II PEEK IBF System - 00191083030692

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-1860-13-6L
In Commercial Distribution


  • 26mm (W) x 11mm (H) x 50mm (L)
38-1860-13-6L

  • Polymeric spinal interbody fusion cage
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