Interpore Cross Intl.
Country not established
- Devices
- 39
What Interpore Cross Intl. makes
Interpore Cross Intl. manufactures spinal fixation and bone graft substitute devices, including resorbable bone graft substitutes like PRO OSTEON, spinal plates (e.g., anterior cervical and fenestrated), rods, screws, and telescopic spacers for thoracolumbar stabilization. Their portfolio also includes imaging systems such as the ALTIUS OCT System for spinal assessment and accessory components like the ACCESS Concentration System for surgical use.
The company’s devices are classified under FDA’s Class II regulatory category and are recorded in the 510(k) clearance registry. These products are intended for orthopedic and spinal applications in the United States.
Catalogue
Search and filter all 39 devicesFrequently asked questions
How many devices does Interpore Cross Intl. have in the registry?
The registry currently lists 39 devices for Interpore Cross Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Interpore Cross Intl.'s devices?
Among its 39 most recently registered devices, Interpore Cross Intl. has devices listed in FDA 510(k) (39 devices).
What risk classes do Interpore Cross Intl.'s devices fall under?
Among its 39 most recently registered devices, the classes recorded for Interpore Cross Intl.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Interpore Cross Intl. in the registry?
The most recently registered devices listed for Interpore Cross Intl. include ALTIUS OCT SYSTEM, MODIFICATION TO SYNERGY SPINAL SYSTEM, PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE and TI FENESTRATED PLATE.