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FDA 510(k)

Spider Frame External Fixation System

K-Number: K170482 · 2017-09-27

ApplicantTasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S
Decision Date2017-09-27
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Spider Frame External Fixation System is a medical device manufactured by Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S. It received FDA 510(k) clearance on 2017-09-27 under approval number K170482. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Spider Frame External Fixation System?

Spider Frame External Fixation System is a medical device that received FDA 510(k) clearance on 2017-09-27. It is manufactured by Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S. The 510(k) number is K170482.

When was Spider Frame External Fixation System approved by the FDA?

Spider Frame External Fixation System received FDA 510(k) clearance on 2017-09-27, under approval number K170482.

What company makes Spider Frame External Fixation System?

Spider Frame External Fixation System is manufactured by Tasarimmed Tibbi Mamuller Sanayi VE Ticaret A.S.

What is the FDA product code for Spider Frame External Fixation System?

The FDA product code for Spider Frame External Fixation System is KTT.

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Related Devices (Code: KTT)

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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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