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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 Class Implantable

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Triad - 00887517053640

8mm Disc Cutter - TLIF
Nuvasive, Inc.
1006825
In Commercial Distribution

  • 00887517053640 ()


  • Orthopaedic implantable-device cutter

Precept - 00887517053251

PRECEPT Screw, 6.5x45mm Poly C.R.
Nuvasive, Inc.
1676545
In Commercial Distribution

  • 00887517053251 ()


  • Bone-screw internal spinal fixation system, non-sterile

MaXcess - 00887517053152

Broach - 14x14mm
Nuvasive, Inc.
1006769
In Commercial Distribution

  • 00887517053152 ()


  • Surgical retraction system, reusable

MaXcess - 00887517053145

Broach - 12x14mm
Nuvasive, Inc.
1006767
In Commercial Distribution

  • 00887517053145 ()


  • Surgical retraction system, reusable

MaXcess - 00887517053138

Broach - 10x14mm
Nuvasive, Inc.
1006765
In Commercial Distribution

  • 00887517053138 ()


  • Surgical retraction system, reusable

MaXcess - 00887517053121

Broach - 8x14mm
Nuvasive, Inc.
1006763
In Commercial Distribution

  • 00887517053121 ()


  • Surgical retraction system, reusable

MaXcess - 00887517053114

6mm Uni-Port Guided Broach 14mm
Nuvasive, Inc.
1006761
In Commercial Distribution

  • 00887517053114 ()


  • Surgical retraction system, reusable

XLP - 00887517053039

XLP Plus Plate, 2+2 Size 16
Nuvasive, Inc.
7534016
In Commercial Distribution

  • 00887517053039 ()


  • Spinal fixation plate, non-bioabsorbable

XLP - 00887517053022

XLP Plus Plate, 2+2 Size 14
Nuvasive, Inc.
7534014
In Commercial Distribution

  • 00887517053022 ()


  • Spinal fixation plate, non-bioabsorbable

XLP - 00887517053015

XLP Plus Plate, 2+2 Size 12
Nuvasive, Inc.
7534012
In Commercial Distribution

  • 00887517053015 ()


  • Spinal fixation plate, non-bioabsorbable
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