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

Show Filters

Femoral Distal Augmentation# 2/16mm-Ti6Al4V
Medacta International SA
02.07.7216FDA
In Commercial Distribution

  • 07630040721509 ()


  • Knee arthroplasty wedge
Femoral Distal Augmentation# 1/20mm-Ti6Al4V
Medacta International SA
02.07.7120FDA
In Commercial Distribution

  • 07630040721448 ()


  • Knee arthroplasty wedge
Femoral Distal Augmentation # 1/4mm-Ti6Al4V
Medacta International SA
02.07.7104FDW
In Commercial Distribution

  • 07630040721387 ()


  • Knee arthroplasty wedge
Femoral Distal Augmentation # 6/8mm-Ti6Al4V
Medacta International SA
02.07.7608FDW
In Commercial Distribution

  • 07630040722353 ()


  • Knee arthroplasty wedge
Augment, Femoral, EXPRT 5MM SZ C
Encore Medical, L.P.
215-0C-005
In Commercial Distribution

  • 00190446180395 ()


  • Knee arthroplasty wedge
Augment, Femoral, EXPRT 5MM SZ D
Encore Medical, L.P.
215-0D-005
In Commercial Distribution

  • 00190446180388 ()


  • Knee arthroplasty wedge
Augment, Femoral, EXPRT 5MM SZ B
Encore Medical, L.P.
215-0B-005
In Commercial Distribution

  • 00190446180371 ()


  • Knee arthroplasty wedge
Augment, Femoral, EXPRT 5MM SZ A
Encore Medical, L.P.
215-0A-005
In Commercial Distribution

  • 00190446180319 ()


  • Knee arthroplasty wedge
ADVANTIM® FEMORAL AUGMENT XLG NON-POROUS
Microport Orthopedics Inc.
18723012
In Commercial Distribution

  • 18723012 ()
  • M684187230121 ()
18723012

  • Knee arthroplasty wedge
ADVANTIM® FEMORAL AUGMENT LG+ NON-POROUS
Microport Orthopedics Inc.
18723010
In Commercial Distribution

  • 18723010 ()
  • M684187230101 ()
18723010

  • Knee arthroplasty wedge
< 1 ... 44 45 46 47 48 ... 143 >