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FDA 510(k)

COMPRESSION CERCLAGE GUNDOLF CCG-GF

K-Number: K973098 · 1997-10-27

ApplicantPlus Orthopedics
Decision Date1997-10-27
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

COMPRESSION CERCLAGE GUNDOLF CCG-GF is the device name listed in this FDA 510(k) record. The listed applicant is Plus Orthopedics. It received FDA 510(k) clearance on 1997-10-27 under 510(k) number K973098. 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 COMPRESSION CERCLAGE GUNDOLF CCG-GF?

COMPRESSION CERCLAGE GUNDOLF CCG-GF is a medical device that received FDA 510(k) clearance on 1997-10-27. The listed applicant is Plus Orthopedics. The 510(k) number is K973098.

When did COMPRESSION CERCLAGE GUNDOLF CCG-GF receive FDA 510(k) clearance?

COMPRESSION CERCLAGE GUNDOLF CCG-GF received FDA 510(k) clearance on 1997-10-27, under 510(k) number K973098.

Who is the listed applicant for COMPRESSION CERCLAGE GUNDOLF CCG-GF?

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

What is the FDA product code for COMPRESSION CERCLAGE GUNDOLF CCG-GF?

The FDA product code for COMPRESSION CERCLAGE GUNDOLF CCG-GF is JDQ.

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Other records listing Plus Orthopedics 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.

K032126PROMOS SHOULDERK033763MODIFICATION TO SLIM GLIDING NAIL SYSTEMK032709MODULAR PLUS HIP STEMK032548IP-XS COMPRESSION NAIL SYSTEMK032215VKS/TC-PLUS REVISION KNEEK032052UC-PLUS SOLUTION UNICONDYLAR KNEE

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Related Devices (Code: JDQ)

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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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