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FDA 510(k)

ANCHORMAN Tibial Ligament Fixation Device

K-Number: K170388 · 2017-07-25

ApplicantSummit Medical , Ltd.
Decision Date2017-07-25
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ANCHORMAN Tibial Ligament Fixation Device is a medical device manufactured by Summit Medical , Ltd.. It received FDA 510(k) clearance on 2017-07-25 under approval number K170388. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANCHORMAN Tibial Ligament Fixation Device?

ANCHORMAN Tibial Ligament Fixation Device is a medical device that received FDA 510(k) clearance on 2017-07-25. It is manufactured by Summit Medical , Ltd.. The 510(k) number is K170388.

When was ANCHORMAN Tibial Ligament Fixation Device approved by the FDA?

ANCHORMAN Tibial Ligament Fixation Device received FDA 510(k) clearance on 2017-07-25, under approval number K170388.

What company makes ANCHORMAN Tibial Ligament Fixation Device?

ANCHORMAN Tibial Ligament Fixation Device is manufactured by Summit Medical , Ltd..

What is the FDA product code for ANCHORMAN Tibial Ligament Fixation Device?

The FDA product code for ANCHORMAN Tibial Ligament Fixation Device is MBI.

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K173110GRAFTSITE

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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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