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FDA 510(k)

2.8 mm/3.3 mm PopLok Suture Anchors

K-Number: K181120 · 2018-12-21

Decision Date2018-12-21
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

2.8 mm/3.3 mm PopLok Suture Anchors is a medical device manufactured by Conmed Corporation. It received FDA 510(k) clearance on 2018-12-21 under approval number K181120. 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 2.8 mm/3.3 mm PopLok Suture Anchors?

2.8 mm/3.3 mm PopLok Suture Anchors is a medical device that received FDA 510(k) clearance on 2018-12-21. It is manufactured by Conmed Corporation. The 510(k) number is K181120.

When was 2.8 mm/3.3 mm PopLok Suture Anchors approved by the FDA?

2.8 mm/3.3 mm PopLok Suture Anchors received FDA 510(k) clearance on 2018-12-21, under approval number K181120.

What company makes 2.8 mm/3.3 mm PopLok Suture Anchors?

2.8 mm/3.3 mm PopLok Suture Anchors is manufactured by Conmed Corporation.

What is the FDA product code for 2.8 mm/3.3 mm PopLok Suture Anchors?

The FDA product code for 2.8 mm/3.3 mm PopLok Suture Anchors is MBI.

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Official Source

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