FDA 510(k)

Cable-Ready® Cable Grip System

Número K: K261271 · 2026-07-16

RequerentePioneer Surgical Technology, Inc.

Data da decisão2026-07-16

Código do produtoJDQ

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Cable-Ready® Cable Grip System is the device name listed in this FDA 510(k) record. The listed applicant is Pioneer Surgical Technology, Inc.. It received FDA 510(k) clearance on 2026-07-16 under 510(k) number K261271. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Cable-Ready® Cable Grip System?

Cable-Ready® Cable Grip System is a medical device that received FDA 510(k) clearance on 2026-07-16. The listed applicant is Pioneer Surgical Technology, Inc.. The 510(k) number is K261271.

When did Cable-Ready® Cable Grip System receive FDA 510(k) clearance?

Cable-Ready® Cable Grip System received FDA 510(k) clearance on 2026-07-16, under 510(k) number K261271.

Who is the listed applicant for Cable-Ready® Cable Grip System?

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

What is the FDA product code for Cable-Ready® Cable Grip System?

The FDA product code for Cable-Ready® Cable Grip System is JDQ.

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Fonte oficial

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