Sternal Cable System
K-Number: K180582 · 2018-05-31
ApplicantA & E Medical Corporation
Decision Date2018-05-31
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Sternal Cable System is a medical device manufactured by A & E Medical Corporation. It received FDA 510(k) clearance on 2018-05-31 under approval number K180582. 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 Sternal Cable System?
Sternal Cable System is a medical device that received FDA 510(k) clearance on 2018-05-31. It is manufactured by A & E Medical Corporation. The 510(k) number is K180582.
When was Sternal Cable System approved by the FDA?
Sternal Cable System received FDA 510(k) clearance on 2018-05-31, under approval number K180582.
What company makes Sternal Cable System?
Sternal Cable System is manufactured by A & E Medical Corporation.
What is the FDA product code for Sternal Cable System?
The FDA product code for Sternal Cable System is JDQ.
Related Clinical Trials
Other Devices by A & E Medical Corporation
Related Devices (Code: JDQ)
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K153242Frontier Medical Devices In-Line Orthopedic Cable Cerclage SystemFrontier Medical Devices, Inc.
K170206Arthrex FiberTape CerclageArthrex, Inc.
K181607Thorecon Rigid Fixation SystemA & E Medical Corporation
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.