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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20 Deg Lordotic Trial, 17mm x 22mm
TITAN SPINE, LLC
7220-1517
Not in Commercial Distribution

  • 00191375042426 ()
7220-1517

  • Spinal implant trial
TRIAL 7220-1516 TLH 20 DEG 22X 16MM
MEDTRONIC SOFAMOR DANEK, INC.
7220-1516
In Commercial Distribution

  • 00191375042419 ()


  • Spinal implant trial
20 Deg Lordotic Trial, 15mm x 22mm
TITAN SPINE, LLC
7220-1515
Not in Commercial Distribution

  • 00191375042402 ()
7220-1515

  • Spinal implant trial
20 Deg Lordotic Trial, 13mm x 22mm
TITAN SPINE, LLC
7220-1513
Not in Commercial Distribution

  • 00191375042389 ()
7220-1513

  • Spinal implant trial
20 Deg Lordotic Trial, 20mm x 18mm
TITAN SPINE, LLC
7220-0520
Not in Commercial Distribution

  • 00191375042365 ()
7220-0520

  • Spinal implant trial
20 Deg Lordotic Trial, 19mm x 18mm
TITAN SPINE, LLC
7220-0519
Not in Commercial Distribution

  • 00191375042358 ()
7220-0519

  • Spinal implant trial
20 Deg Lordotic Trial, 18mm x 18mm
TITAN SPINE, LLC
7220-0518
Not in Commercial Distribution

  • 00191375042341 ()
7220-0518

  • Spinal implant trial
20 Deg Lordotic Trial, 17mm x 18mm
TITAN SPINE, LLC
7220-0517
Not in Commercial Distribution

  • 00191375042334 ()
7220-0517

  • Spinal implant trial
20 Deg Lordotic Trial, 16mm x 18mm
TITAN SPINE, LLC
7220-0516
Not in Commercial Distribution

  • 00191375042327 ()
7220-0516

  • Spinal implant trial
20 Deg Lordotic Trial, 15mm x 18mm
TITAN SPINE, LLC
7220-0515
Not in Commercial Distribution

  • 00191375042310 ()
7220-0515

  • Spinal implant trial
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