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FDA 510(k)

CODMAN SOF'WIRE TITANIUM CABLE SYSTEM

K-Number: K923869 · 1993-05-12

ApplicantCodman & Shurtleff, Inc.
Decision Date1993-05-12
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CODMAN SOF'WIRE TITANIUM CABLE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1993-05-12 under 510(k) number K923869. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODMAN SOF'WIRE TITANIUM CABLE SYSTEM?

CODMAN SOF'WIRE TITANIUM CABLE SYSTEM is a medical device that received FDA 510(k) clearance on 1993-05-12. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K923869.

When did CODMAN SOF'WIRE TITANIUM CABLE SYSTEM receive FDA 510(k) clearance?

CODMAN SOF'WIRE TITANIUM CABLE SYSTEM received FDA 510(k) clearance on 1993-05-12, under 510(k) number K923869.

Who is the listed applicant for CODMAN SOF'WIRE TITANIUM CABLE SYSTEM?

The FDA 510(k) record lists Codman & Shurtleff, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CODMAN SOF'WIRE TITANIUM CABLE SYSTEM?

The FDA product code for CODMAN SOF'WIRE TITANIUM CABLE SYSTEM is JDQ.

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Other records listing Codman & Shurtleff, Inc. as applicant

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Related Devices (Code: JDQ)

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.

K261271Cable-Ready® Cable Grip SystemPioneer Surgical Technology, Inc.K243905Stitch Cerclage – Suture TapesGM Dos Reis Industria e Comercio Ltda.K243344Arthrex FiberTape and TigerTape Cerclage Sutures; Arthrex Radiopaque FiberTape Cerclage SuturesArthrex, Inc.K232733Mbrace CableMedacta International S.A.K233949ACCORD Cable SystemSmith & Nephew, Inc.K232986VariTrax Sternal CircumFixation SystemCircumfix Solutions, 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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