Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2016-01-15 under 510(k) 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. The listed applicant is Zimmer, Inc.. The 510(k) number is K151848.

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

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

Who is the listed applicant for Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System?

The FDA 510(k) record lists Zimmer, 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: 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.

Other records listing Zimmer, Inc. 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.

PMA P060037Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearingK261683Augment Off-Axis Instrument SystemK260831Z1 Hip SystemK251840Zimmer® Persona® Personalized Knee SystemK260182Avenir® Müller Stem; Avenir Complete™ Hip SystemK253592Zimmer Biomet Reverse Shoulder Prosthesis (Alliance Humeral Bearings, Identity Humeral Trays, Comprehensive Reverse Humeral Trays, Comprehensive Reverse 32mm Glenospheres and Adapter)

View all 80 devices →

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.

↑