SEARCH RESULTS FOR: seaspine(22323 results)

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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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IMPLANT, 22mm LG, 12-18mm HT, 10mm WD, 0 DEG
SEASPINE ORTHOPEDICS CORPORATION
82-2212
In Commercial Distribution

  • 10889981123451 ()

  • 22mm LG, 12-18mm HT, 10mm WD, 0 Deg
82-2212

  • Vertebral body prosthesis, non-sterile
IMPLANT, 22mm LG, 10-15mm HT, 10mm WD, 0 DEG
SEASPINE ORTHOPEDICS CORPORATION
82-2210
In Commercial Distribution

  • 10889981123444 ()

  • 22mm LG, 10-15mm HT, 10mm WD, 0 Deg
82-2210

  • Vertebral body prosthesis, non-sterile
IMPLANT, 22mm LG, 8-12mm HT, 10mm WD, 0 DEG
SEASPINE ORTHOPEDICS CORPORATION
82-2208
In Commercial Distribution

  • 10889981123437 ()

  • 22mm LG, 8-12mm HT, 10mm WD, 0 Deg
82-2208

  • Vertebral body prosthesis, non-sterile
Expandable IBD Implants
SEASPINE ORTHOPEDICS CORPORATION
EXPIMP
In Commercial Distribution

  • 10889981123420 ()
EXPIMP

  • Instrument tray, reusable
Inserter
SEASPINE ORTHOPEDICS CORPORATION
98-2005
In Commercial Distribution

  • 10889981120764 ()
98-2005

  • Orthopaedic implant inserter/extractor, reusable
SeaSpine Bi-Ostetic Cancellous Blocks is a mixture with a nominal composition of 60% hydroxyapatite and 40% beta-tri-calcium phosphate. SeaSpine Bi-Ostetic Cancellous Blocks is safe and has excellent biocompatibility. After it is implanted, the implant resorbs and is later replaced by natural bone. SeaSpine Bi-Ostetic Cancellous Blocks is a natural choice for sparing patients the trauma of autograft harvesting. It also provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission. SeaSpine Bi-Ostetic Cancellous Blocks is an osteoconductive bone substitute shaped as blocks that are intended to be used to fill voids and gaps that are not intrinsic to the stability of the bone structure. These gaps or voids may be located in the extremities, spine, pelvis, or cranium. The blocks may be pressed into the void or into the surgical site by hand. The SeaSpine Bi-Ostetic Cancellous Blocks provide void filling material that acts as a temporary support medium. The blocks are not intended to provide structural support during the healing process. The implant is radio-opaque. SeaSpine Bi-Ostetic Cancellous Blocks is biocompatible and resorbs in the body as bone ingrowth occurs.
BERKELEY ADVANCED BIOMATERIALS, LLC
SBiO-XYZ400606P
In Commercial Distribution

  • 00858418003966 ()
SBiO-XYZ400606P

  • Bone matrix implant, synthetic, non-antimicrobial
No Description
LUMITEX, INC.
007979
In Commercial Distribution

  • 00812432022891 ()
91-8412

  • Fibreoptic light cable
No Description
LUMITEX, INC.
007978
In Commercial Distribution

  • 00812432022884 ()
91-8411

  • Fibreoptic light cable
No Description
LUMITEX, INC.
007977
In Commercial Distribution

  • 00812432022877 ()
91-8410

  • Fibreoptic light cable
No Description
LUMITEX, INC.
007976
In Commercial Distribution

  • 00812432022860 ()
91-8409

  • Fibreoptic light cable
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