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FDA 510(k)

aprevo® anterior lumbar interbody fusion device with interfixation

K-Number: K241477 · 2024-10-09

ApplicantCarlsmed, Inc.
Decision Date2024-10-09
Product CodeOVD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

aprevo® anterior lumbar interbody fusion device with interfixation is a medical device manufactured by Carlsmed, Inc.. It received FDA 510(k) clearance on 2024-10-09 under approval number K241477. The device is classified under product code OVD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the aprevo® anterior lumbar interbody fusion device with interfixation?

aprevo® anterior lumbar interbody fusion device with interfixation is a medical device that received FDA 510(k) clearance on 2024-10-09. It is manufactured by Carlsmed, Inc.. The 510(k) number is K241477.

When was aprevo® anterior lumbar interbody fusion device with interfixation approved by the FDA?

aprevo® anterior lumbar interbody fusion device with interfixation received FDA 510(k) clearance on 2024-10-09, under approval number K241477.

What company makes aprevo® anterior lumbar interbody fusion device with interfixation?

aprevo® anterior lumbar interbody fusion device with interfixation is manufactured by Carlsmed, Inc..

What is the FDA product code for aprevo® anterior lumbar interbody fusion device with interfixation?

The FDA product code for aprevo® anterior lumbar interbody fusion device with interfixation is OVD.

Related Clinical Trials

NCT07301385 Evaluation of Head-Mounted Spatial Computing and Three-Dimensional (3D) Visualization in Ocular Microsurgery: A Safety and Workflow Study ACTIVE_NOT_RECRUITING NCT07222787 Post-market Safety and Effectiveness of the CORUS-LX System in Improving Lumbar Interbody Fusion Outcomes RECRUITING NCT07610850 Brain-controlled Spinal Cord Stimulation in Participants With Chronic Stroke for Lower and Upper Limb Rehabilitation NOT_YET_RECRUITING NCT06462729 LDGraft in Single Level Anterior Lumbar Interbody Fusion (ALIF) RECRUITING NCT05438719 MOTUS Total Joint Replacement Investigational Device Exemption Study ACTIVE_NOT_RECRUITING NCT06540807 SafeHeal Anastomosis Feasibility Evaluation (SAFE)-2023 Study COMPLETED

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: 38569929 Utilization of Bone-Anchored Annular Defect Closure to Prevent Reherniation Following Lumbar Discectomy: Overcoming Barriers to Clinical Adoption and Market Access. International journal of spine surgery (2024) PMID: 38273730 Ten-Year Risk of Recall of Novel Spine Devices. Spine (2024) PMID: 26056630 Therapeutic sustainability and durability of coflex interlaminar stabilization after decompression for lumbar spinal stenosis: a four year assessment. International journal of spine surgery (2015)

Other Devices by Carlsmed, Inc.

K202034aprevo Intervertebral Body Fusion Device K210542aprevo Transforaminal IBF K222195aprevo® Digital Workflow K222009aprevo® anterior lumbar interbody fusion device with interfixation K222082aprevo® anterior and lateral lumbar interbody fusion devices, aprevo® transforaminal lumbar interbody fusion devices K231955aprevo® Digital Segmentation

View all 21 devices →

Related Devices (Code: OVD)

K162680SOVEREIGN® Spinal SystemMedtronic Sofamor Danek USA, Inc. K162351SeaSpine® Vu a•POD™ Prime NanoMetalene® Intervertebral Body Fusion DeviceSeaSpine Orthopedics Corporation K161993Leva® Anterior Interbody SystemSpine Wave, Inc. K161379ELSA SpacersGlobus Medical, Inc. K161173Avenue® T TLIF CageLdr Spine USA, Inc. K161129PILLAR SA PTCOrthofix, 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.

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