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)

ARC SURGICAL RESORBABLE COMPRESSION SCREW SYSTEM

K-Number: K043176 · 2005-06-17

ApplicantArc Surgical, LLC
Decision Date2005-06-17
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARC SURGICAL RESORBABLE COMPRESSION SCREW SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Arc Surgical, LLC. It received FDA 510(k) clearance on 2005-06-17 under 510(k) number K043176. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARC SURGICAL RESORBABLE COMPRESSION SCREW SYSTEM?

ARC SURGICAL RESORBABLE COMPRESSION SCREW SYSTEM is a medical device that received FDA 510(k) clearance on 2005-06-17. The listed applicant is Arc Surgical, LLC. The 510(k) number is K043176.

When did ARC SURGICAL RESORBABLE COMPRESSION SCREW SYSTEM receive FDA 510(k) clearance?

ARC SURGICAL RESORBABLE COMPRESSION SCREW SYSTEM received FDA 510(k) clearance on 2005-06-17, under 510(k) number K043176.

Who is the listed applicant for ARC SURGICAL RESORBABLE COMPRESSION SCREW SYSTEM?

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

What is the FDA product code for ARC SURGICAL RESORBABLE COMPRESSION SCREW SYSTEM?

The FDA product code for ARC SURGICAL RESORBABLE COMPRESSION SCREW SYSTEM is HWC. This falls under the Cardiovascular category.

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 Arc Surgical, 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.

K071616ARC SURGICAL BIOTRAK PIN SYSTEMK063244ARC SURGICAL BONE REDUCTION SCREWK061763ARC SURGICAL BIOTRAK SCREW

Related Devices (Code: HWC)

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.

K262975Arthrex Beaming SystemArthrex, Inc.K260995DynaNail Helix® Fixation SystemMedShape, Inc.K254280F.A.S.T ScrewSteps OrthoK261057ActivaScrew™ Cannulated COMBioretec, Ltd.K260106OsteoCoil™ GT Active Compression SystemFlower Orthopedics Corporation DBA Conventus Flower OrthopedK262344Large Compression ScrewsTriMed, 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.

↑