FDA 510(k)

Ortus Expandable Lumbar Interbody Fusion System

K-Number: K172334 · 2017-10-25

Decision Date2017-10-25

Product CodeMAX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Ortus Expandable Lumbar Interbody Fusion System is a medical device manufactured by Atlas Spine, Inc.. It received FDA 510(k) clearance on 2017-10-25 under approval number K172334. 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 Ortus Expandable Lumbar Interbody Fusion System?

Ortus Expandable Lumbar Interbody Fusion System is a medical device that received FDA 510(k) clearance on 2017-10-25. It is manufactured by Atlas Spine, Inc.. The 510(k) number is K172334.

When was Ortus Expandable Lumbar Interbody Fusion System approved by the FDA?

Ortus Expandable Lumbar Interbody Fusion System received FDA 510(k) clearance on 2017-10-25, under approval number K172334.

What company makes Ortus Expandable Lumbar Interbody Fusion System?

Ortus Expandable Lumbar Interbody Fusion System is manufactured by Atlas Spine, Inc..

What is the FDA product code for Ortus Expandable Lumbar Interbody Fusion System?

The FDA product code for Ortus Expandable Lumbar Interbody Fusion System is MAX.

Related Clinical Trials

NCT07222787 Post-market Safety and Effectiveness of the CORUS-LX System in Improving Lumbar Interbody Fusion Outcomes RECRUITING NCT05508360 "Lumbar Operatively Inserted PerQdisc Artificial Implant Following Nulcectomy" (LOPAIN2) RECRUITING NCT06462729 LDGraft in Single Level Anterior Lumbar Interbody Fusion (ALIF) RECRUITING NCT05438719 MOTUS Total Joint Replacement Investigational Device Exemption Study ACTIVE_NOT_RECRUITING NCT04823858 3Spine Lumbar Fusion Real World Evidence Study ACTIVE_NOT_RECRUITING NCT05762055 Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOCK Osseointegrative Technology ENROLLING_BY_INVITATION

Related PubMed Literature

PMID: 41839575 A Perspective for Integrating Real-World Evidence Into the Investigational Device Exemption Study Design for Lumbar Total Joint Replacement. International journal of spine surgery (2026) PMID: 41166829 Assessment of intra-operative impact durability of additively manufactured mock lumbar intervertebral body fusion devices. Journal of biomechanics (2026)

Other Devices by Atlas Spine, Inc.

K162918Atlas Spine Expandable Interbody System K182418V3 Segmental Plating System K180675Atlas Spine Expandable Cervical Interbody System K202302Atlas Spine Rebar (Ti) Spacer System K192570Atlas Spine Expandable Cervical Standalone Interbody System K243191Atlas Spine Lateral Expandable Interbody System

View all 9 devices →

Related Devices (Code: MAX)

K163180Hubble IIOrbbo Surgical, LLC K162446FORZA Spacer System, PILLAR PEEK Spacer System, PILLAR SA PEEK Spacer System, SKYHAWK Lateral Interbody Fusion SystemOrthofix, Inc. K162327COUGAR® LS Lateral Cage System and COUGAR® SystemMedos International SARL K162103Choice Spine Lumbar Spacer System (Sabre, Shark, Hornet, Harpoon), Choice Spine Interbody Fusion System (Harrier), Choice Spine Vertebral Body Replacement System (Hawkeye)Choicespine, LP K162431Luna 3D Interbody Fusion SystemBenvenue Medical, Inc. K160959Xsert Lumbar Expandable Interbody SystemX-Spine Systems, Inc.

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.