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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 Class Implantable

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MLX - 00887517660527

Universal Torque Handle, 22 in-lb
Nuvasive, Inc.
1642582
In Commercial Distribution

  • 00887517660527 ()


  • Surgical instrument handle, non-torque-limiting

MLX - 00887517660503

MLX Graft Containment Plate Inserter
Nuvasive, Inc.
1642570
In Commercial Distribution

  • 00887517660503 ()


  • Orthopaedic implant inserter/extractor, reusable

PEEK Corpectomy - 00887517659880

PEEK Corpectomy Driver, Railed
Nuvasive, Inc.
5987004
In Commercial Distribution

  • 00887517659880 ()


  • Orthopaedic implant driver

Armada - 00887517659859

Armada Gearshift Probe, Cannulated
Nuvasive, Inc.
7451062
In Commercial Distribution

  • 00887517659859 ()


  • Internal spinal fixation procedure kit, reusable

Fulfill - 00887517659705

Fulfill Dilator, Second TP Access
Nuvasive, Inc.
10000984
In Commercial Distribution

  • 00887517659705 ()


  • Internal spinal fixation procedure kit, reusable

Fulfill - 00887517659187

Fulfill C-C Retractor, 5" Straight
Nuvasive, Inc.
10000973
In Commercial Distribution

  • 00887517659187 ()


  • Surgical retraction system, reusable

NuVasive - 00887517658357

Universal Distractor, Multi-Level
Nuvasive, Inc.
1111702
In Commercial Distribution

  • 00887517658357 ()


  • Orthopaedic surgical distractor, internal

ReLine - 00887517658104

RELINE HS Screwdriver
Nuvasive, Inc.
10000992
In Commercial Distribution

  • 00887517658104 ()


  • Surgical screwdriver, reusable

MaXcess - 00887517528223

MaXcess MAS TLIF Retractor, Solid
Nuvasive, Inc.
1628450
In Commercial Distribution

  • 00887517528223 ()


  • Surgical retraction system, reusable

MaXcess - 00887517528216

MaXcess MAS TLIF Retractor, Flexible
Nuvasive, Inc.
1628400
In Commercial Distribution

  • 00887517528216 ()


  • Surgical retraction system, reusable
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