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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 - 00191083031743

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2270-9-6L
In Commercial Distribution

  • 00191083031743 ()

  • 22mm (W) x 9mm (H) x 70mm (L) x 6 Degrees Lordosis
38-2270-9-6L

  • Polymeric spinal interbody fusion cage

V. Mueller - 10885403019654

GENESIS EXTRA-LONG CONTAINER 25 X 12 inches 63.5 X 30.5CM 6 inches 15.2CM DEEP SOLID BOTTOM
STERIS CORPORATION
CD7-6C
In Commercial Distribution

  • 10885403019654 ()
CD76C

  • Device sterilization/disinfection container, reusable

Cross-Fuse® II PEEK IBF System - 00191083031729

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2270-17-18L
In Commercial Distribution

  • 00191083031729 ()

  • 22mm (W) x 17mm (H) x 70mm (L) x 18 Degrees Lordosis
38-2270-17-18L

  • Polymeric spinal interbody fusion cage

Cross-Fuse® II PEEK IBF System - 00191083031712

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2270-17-12L
In Commercial Distribution

  • 00191083031712 ()

  • 22mm (W) x 17mm (H) x 70mm (L) x 12 Degrees Lordosis
38-2270-17-12L

  • Polymeric spinal interbody fusion cage

V. Mueller - 10885403019616

GENESIS RETRACTOR CONTAINER 26 X 17 inches 66 X 43.2CM 6 inches 15.2CM DEEP SOLID BOTTOM
STERIS CORPORATION
CD6-6C
In Commercial Distribution

  • 10885403019616 ()
CD66C

  • Device sterilization/disinfection container, reusable

Cross-Fuse® II PEEK IBF System - 00191083031699

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2270-15-18L
In Commercial Distribution

  • 00191083031699 ()

  • 22mm (W) x 15mm (H) x 70mm (L) x 18 Degrees Lordosis
38-2270-15-18L

  • Polymeric spinal interbody fusion cage

V. Mueller - 10885403019593

V. Mueller GENESIS LARGE, CONTAINER 28 X 11" (71.1 X 27.9CM) 6" (15.2CM) DEEP, PERFORATED STERRAD COMPATIBLE
CAREFUSION 2200, INC
CD5-61ST
Not in Commercial Distribution

  • 10885403019593 ()
CD5-61ST

  • Device sterilization/disinfection container, reusable

Cross-Fuse® II PEEK IBF System - 00191083031675

INTERBODY FUSION DEVICE
Rti Surgical, Inc.
38-2270-13-6L
In Commercial Distribution

  • 00191083031675 ()

  • 22mm (W) x 13mm (H) x 70mm (L) x 6 Degrees Lordosis
38-2270-13-6L

  • Polymeric spinal interbody fusion cage

V. Mueller - 10885403019579

V. Mueller GENESIS LARGE ENDO CONTAINER 28 X 11" (71.1 X 27.9CM) 6" (15.2CM) DEEP PERFORATED BOTTOM
CAREFUSION 2200, INC
CD5-61B
Not in Commercial Distribution

  • 10885403019579 ()
CD5-61B

  • Device sterilization/disinfection container, reusable

V. Mueller - 10885403019562

V. Mueller GENESIS LARGE, SHALLOW CONT. 28 X 11" (71.1 X 27.9CM) 3" (7.6CM) DEEP, PERFORATED STERRAD COMPATIBLE
CAREFUSION 2200, INC
CD5-3ST
Not in Commercial Distribution

  • 10885403019562 ()
CD5-3ST

  • Device sterilization/disinfection container, reusable
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