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FDA 510(k)

Cable-Ready® Cable Grip System

K-Number: K261271 · 2026-07-16

ApplicantPioneer Surgical Technology, Inc.
Decision Date2026-07-16
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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.

Other records listing Pioneer Surgical Technology, 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.

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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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