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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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Stand-Alone Cervical Interbody Fusion Device
Pioneer Surgical Technology, Inc.
63-1616-6-7L
Not in Commercial Distribution

  • 00846468075255 ()
63-1616-6-7L

  • Polymeric spinal interbody fusion cage
Stand-Alone Cervical Interbody Fusion Device
Pioneer Surgical Technology, Inc.
63-1614-12-7L
Not in Commercial Distribution

  • 00846468075248 ()
63-1614-12-7L

  • Polymeric spinal interbody fusion cage
Stand-Alone Cervical Interbody Fusion Device
Pioneer Surgical Technology, Inc.
63-1614-11-7L
Not in Commercial Distribution

  • 00846468075231 ()
63-1614-11-7L

  • Polymeric spinal interbody fusion cage
PEEK Interbody Fusion Cage
BAUI BIOTECH CO. LTD.
595-18328
In Commercial Distribution

  • 04718005152414 ()


  • Polymeric spinal interbody fusion cage
PEEK Interbody Fusion Cage
BAUI BIOTECH CO. LTD.
595-17328
In Commercial Distribution

  • 04718005152407 ()


  • Polymeric spinal interbody fusion cage
PEEK Interbody Fusion Cage
BAUI BIOTECH CO. LTD.
595-16328
In Commercial Distribution

  • 04718005152391 ()


  • Polymeric spinal interbody fusion cage
PEEK Interbody Fusion Cage
BAUI BIOTECH CO. LTD.
595-15328
In Commercial Distribution

  • 04718005152384 ()


  • Polymeric spinal interbody fusion cage
PEEK Interbody Fusion Cage
BAUI BIOTECH CO. LTD.
595-14328
In Commercial Distribution

  • 04718005152377 ()


  • Polymeric spinal interbody fusion cage
PEEK Interbody Fusion Cage
BAUI BIOTECH CO. LTD.
595-13328
In Commercial Distribution

  • 04718005152360 ()


  • Polymeric spinal interbody fusion cage
PEEK Interbody Fusion Cage
BAUI BIOTECH CO. LTD.
595-12328
In Commercial Distribution

  • 04718005152353 ()


  • Polymeric spinal interbody fusion cage
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