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FDA 510(k)

ARC SURGICAL BONE REDUCTION SCREW

K-Number: K063244 · 2006-12-27

ApplicantArc Surgical, LLC
Decision Date2006-12-27
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARC SURGICAL BONE REDUCTION SCREW 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 2006-12-27 under 510(k) number K063244. 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 BONE REDUCTION SCREW?

ARC SURGICAL BONE REDUCTION SCREW is a medical device that received FDA 510(k) clearance on 2006-12-27. The listed applicant is Arc Surgical, LLC. The 510(k) number is K063244.

When did ARC SURGICAL BONE REDUCTION SCREW receive FDA 510(k) clearance?

ARC SURGICAL BONE REDUCTION SCREW received FDA 510(k) clearance on 2006-12-27, under 510(k) number K063244.

Who is the listed applicant for ARC SURGICAL BONE REDUCTION SCREW?

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 BONE REDUCTION SCREW?

The FDA product code for ARC SURGICAL BONE REDUCTION SCREW 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.

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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 SYSTEMK061763ARC SURGICAL BIOTRAK SCREWK043176ARC SURGICAL RESORBABLE COMPRESSION SCREW SYSTEM

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.

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