Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ATALIA TITANIUM SURGICAL MESH

K-Number: K041798 · 2005-02-07

ApplicantUs Spinal Technologies, LLC
Decision Date2005-02-07
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ATALIA TITANIUM SURGICAL MESH is the device name listed in this FDA 510(k) record. The listed applicant is Us Spinal Technologies, LLC. It received FDA 510(k) clearance on 2005-02-07 under 510(k) number K041798. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATALIA TITANIUM SURGICAL MESH?

ATALIA TITANIUM SURGICAL MESH is a medical device that received FDA 510(k) clearance on 2005-02-07. The listed applicant is Us Spinal Technologies, LLC. The 510(k) number is K041798.

When did ATALIA TITANIUM SURGICAL MESH receive FDA 510(k) clearance?

ATALIA TITANIUM SURGICAL MESH received FDA 510(k) clearance on 2005-02-07, under 510(k) number K041798.

Who is the listed applicant for ATALIA TITANIUM SURGICAL MESH?

The FDA 510(k) record lists Us Spinal Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ATALIA TITANIUM SURGICAL MESH?

The FDA product code for ATALIA TITANIUM SURGICAL MESH is MQP.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Us Spinal Technologies, LLC as applicant

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.

K041625LTD POLYAXIAL FIXATION SYSTEM

Related Devices (Code: MQP)

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.

K261810Vertiwedge® Intraosseous SystemFoundation Surgical GroupK261031POSEIDON STSignus Medinzintechnik GmbHK253158VyBrate™ VBR SystemVy Spine, LLCK241468Vertiwedge® Intraosseous SystemFoundation Surgical Group, Inc.K232790KONG®-TL VBR System and KONG® C VBR SystemIcotec AGK233359DOMINION Expandable Corpectomy SystemAstura Medical

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.

↑