Thorecon Rigid Fixation System
K-Number: K181607 · 2018-10-12
ApplicantA & E Medical Corporation
Decision Date2018-10-12
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Thorecon Rigid Fixation System is a medical device manufactured by A & E Medical Corporation. It received FDA 510(k) clearance on 2018-10-12 under approval number K181607. 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 Thorecon Rigid Fixation System?
Thorecon Rigid Fixation System is a medical device that received FDA 510(k) clearance on 2018-10-12. It is manufactured by A & E Medical Corporation. The 510(k) number is K181607.
When was Thorecon Rigid Fixation System approved by the FDA?
Thorecon Rigid Fixation System received FDA 510(k) clearance on 2018-10-12, under approval number K181607.
What company makes Thorecon Rigid Fixation System?
Thorecon Rigid Fixation System is manufactured by A & E Medical Corporation.
What is the FDA product code for Thorecon Rigid Fixation System?
The FDA product code for Thorecon Rigid Fixation 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.