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FDA 510(k)

WROBLEWSKI SPRING COMPRESSION WIRE SYSTEM

K-Number: K882890 · 1988-08-08

ApplicantThackray USA
Decision Date1988-08-08
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WROBLEWSKI SPRING COMPRESSION WIRE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Thackray USA. It received FDA 510(k) clearance on 1988-08-08 under 510(k) number K882890. 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 WROBLEWSKI SPRING COMPRESSION WIRE SYSTEM?

WROBLEWSKI SPRING COMPRESSION WIRE SYSTEM is a medical device that received FDA 510(k) clearance on 1988-08-08. The listed applicant is Thackray USA. The 510(k) number is K882890.

When did WROBLEWSKI SPRING COMPRESSION WIRE SYSTEM receive FDA 510(k) clearance?

WROBLEWSKI SPRING COMPRESSION WIRE SYSTEM received FDA 510(k) clearance on 1988-08-08, under 510(k) number K882890.

Who is the listed applicant for WROBLEWSKI SPRING COMPRESSION WIRE SYSTEM?

The FDA 510(k) record lists Thackray USA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WROBLEWSKI SPRING COMPRESSION WIRE SYSTEM?

The FDA product code for WROBLEWSKI SPRING COMPRESSION WIRE SYSTEM is JDQ.

Related Clinical Trials

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Other records listing Thackray USA 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.

K871867ELITE MODULAR HIP SYSTEMK871852COXA ACETABULAR CUPK863554THACKRAY CRUCIATE SPARING KNEE CS-1K855166THACKRAY TOTAL CONDYLAR KNEES

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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