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FDA 510(k)

Anterior Spine Truss System (STS) Interbody Fusion Device

K-Number: K170851 · 2017-08-07

Applicant4Web, Inc.
Decision Date2017-08-07
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Anterior Spine Truss System (STS) Interbody Fusion Device is a medical device manufactured by 4Web, Inc.. It received FDA 510(k) clearance on 2017-08-07 under approval number K170851. 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 Anterior Spine Truss System (STS) Interbody Fusion Device?

Anterior Spine Truss System (STS) Interbody Fusion Device is a medical device that received FDA 510(k) clearance on 2017-08-07. It is manufactured by 4Web, Inc.. The 510(k) number is K170851.

When was Anterior Spine Truss System (STS) Interbody Fusion Device approved by the FDA?

Anterior Spine Truss System (STS) Interbody Fusion Device received FDA 510(k) clearance on 2017-08-07, under approval number K170851.

What company makes Anterior Spine Truss System (STS) Interbody Fusion Device?

Anterior Spine Truss System (STS) Interbody Fusion Device is manufactured by 4Web, Inc..

What is the FDA product code for Anterior Spine Truss System (STS) Interbody Fusion Device?

The FDA product code for Anterior Spine Truss System (STS) Interbody Fusion Device is MAX.

Related Clinical Trials

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Related PubMed Literature

PMID: 42201559 Time-series and thematic analyses of clinical utilities and operational issues in early clinical studies of the da Vinci surgical system. Journal of robotic surgery (2026) PMID: 42175114 Make Open Source Compliant: Validation in Non-Interventional Clinical Studies. Studies in health technology and informatics (2026) PMID: 42174947 Aligning AI-Native 6G Healthcare Systems with EU Ethical and Legal Frameworks. Studies in health technology and informatics (2026) PMID: 41879133 Medical Device Regulation - Who Does the FDA Serve? The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics (2026)

Other Devices by 4Web, Inc.

K153436LATERAL Spine Truss System K172392Lateral Spinal Truss System (LSTS) Interbody Fusion Device K171351Posterior Spine Truss System (PSTS) Interbody Fusion Device K172294Osteotomy Truss System (OTS) K173159Cervical Spinal Truss System (CSTS) Interbody Fusion Device K190870Cervical Spinal Truss System-Stand Alone (CSTS-SA)

View all 11 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.

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