Camber Spine Technologies, LLC FDA Approvals

0 new drug approvals and 3 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Alcantara Thoracolumbar Plate System510(k)Apr 16, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Apr 16, 2024
Camber Sacroiliac (SI) Fixation System510(k)Sep 2, 2022Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Sep 2, 2022
SPIRA-T Oblique Posterior Lumbar Spacers, SPIRA-P Posterior Lumbar Spacers510(k)Jun 15, 2021Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Jun 15, 2021