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FDA 510(k)

Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System

K-Number: K151848 · 2016-01-15

ApplicantZimmer, Inc.
Decision Date2016-01-15
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System is a medical device manufactured by Zimmer, Inc.. It received FDA 510(k) clearance on 2016-01-15 under approval number K151848. 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 Pin System, Cable-Ready Needle System?

Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System is a medical device that received FDA 510(k) clearance on 2016-01-15. It is manufactured by Zimmer, Inc.. The 510(k) number is K151848.

When was Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System approved by the FDA?

Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System received FDA 510(k) clearance on 2016-01-15, under approval number K151848.

What company makes Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System?

Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System is manufactured by Zimmer, Inc..

What is the FDA product code for Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System?

The FDA product code for Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System is JDQ.

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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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