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Curiteva, Inc. FDA Approvals

0 new drug approvals and 10 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
Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; Curiteva Porous PEEK Laminoplasty System; Curiteva Porous PEEK Standalone ALIF System510(k)Jan 16, 2026Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Jan 16, 2026
Curiteva Porous PEEK Cervical Interbody Fusion System510(k)Jan 15, 2026Orthopedic	Orthopedic	510(k)Substantially Equivalent (Special)	Jan 15, 2026
Curiteva Porous PEEK Standalone ALIF System510(k)Jun 18, 2025Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Jun 18, 2025
Curiteva Porous PEEK Laminoplasty System510(k)Oct 28, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Special)	Oct 28, 2024
Curiteva Thoracolumbar Plate System510(k)Feb 29, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Feb 29, 2024
Curiteva Porous PEEK Lumbar Interbody Fusion System510(k)Jan 18, 2024Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Jan 18, 2024
Curiteva Laminoplasty System510(k)Jun 28, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Jun 28, 2023
Curiteva Porous PEEK Cervical Interbody Fusion System510(k)Feb 13, 2023Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Feb 13, 2023
Curiteva Navigation System510(k)Jan 6, 2023Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Jan 6, 2023
Curiteva Sacroiliac Joint Fusion System510(k)Sep 9, 2021Orthopedic	Orthopedic	510(k)Substantially Equivalent (Traditional)	Sep 9, 2021

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