FDA 510(k)

ORIA NATURA SPACER

K-Number: K073669 · 2008-02-13

Decision Date2008-02-13

Product CodeMAX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

ORIA NATURA SPACER is the device name listed in this FDA 510(k) record. The listed applicant is Choicespine, LP. It received FDA 510(k) clearance on 2008-02-13 under 510(k) number K073669. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORIA NATURA SPACER?

ORIA NATURA SPACER is a medical device that received FDA 510(k) clearance on 2008-02-13. The listed applicant is Choicespine, LP. The 510(k) number is K073669.

When did ORIA NATURA SPACER receive FDA 510(k) clearance?

ORIA NATURA SPACER received FDA 510(k) clearance on 2008-02-13, under 510(k) number K073669.

Who is the listed applicant for ORIA NATURA SPACER?

The FDA 510(k) record lists Choicespine, LP as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORIA NATURA SPACER?

The FDA product code for ORIA NATURA SPACER is MAX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Choicespine, LP as applicant

K190227Boomerang™ Anterior Cervical Plate System K183397ChoiceSpine Stealth Cervical Spacer System K182721Choice Spine Navigation System K183214Raven Lumbar Plate System K180519HARRIER-SA™ Lumbar Interbody System K172816TiGer Shark™ System

View all 19 devices →

Related Devices (Code: MAX)

K261049SCALA® TLSpineart SA K261430TruLift Expandable SystemLife Spine, Inc.K253011Catalyft PL Expandable Interbody SystemMedtronic Sofamor Danek USA, Inc.K261020Symmetrix™ L Spinal SystemMedtronic Sofamor Danek USA, Inc.K253420Admiral ACP System; Explorer TO System; Laminoplasty System; Manta Ray TDF Spacer; Meridian Interbody System; Meridian Anterior Plate System; Reef L Interbody System; Reef TO/TA System; Regatta Lateral System; Regatta Lateral Plate System; Shoreline ACS Interbody System; Shoreline Threaded TruProfile Plate; Shoreline RT Interbody System; Vu Mesh; WaveForm A Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TA Interbody System; WaveForm TO Interbody SySeaSpine Orthopedics Corporation K253151Fule Interbody Fusion Cage SystemBeijing Fule Science & Technology Development Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.