TELIX K Interbody System
K-Number: K170890 · 2017-06-02
ApplicantBiedermann Motech GmbH & Co. KG
Decision Date2017-06-02
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
TELIX K Interbody System is a medical device manufactured by Biedermann Motech GmbH & Co. KG. It received FDA 510(k) clearance on 2017-06-02 under approval number K170890. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the TELIX K Interbody System?
TELIX K Interbody System is a medical device that received FDA 510(k) clearance on 2017-06-02. It is manufactured by Biedermann Motech GmbH & Co. KG. The 510(k) number is K170890.
When was TELIX K Interbody System approved by the FDA?
TELIX K Interbody System received FDA 510(k) clearance on 2017-06-02, under approval number K170890.
What company makes TELIX K Interbody System?
TELIX K Interbody System is manufactured by Biedermann Motech GmbH & Co. KG.
What is the FDA product code for TELIX K Interbody System?
The FDA product code for TELIX K Interbody System is MAX.
Related Clinical Trials
Other Devices by Biedermann Motech GmbH & Co. KG
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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.