FDA 510(k)

Stryker Self-Punching ICONIX

K-Number: K172921 · 2017-11-20

Decision Date2017-11-20

Product CodeMBI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

Stryker Self-Punching ICONIX is a medical device manufactured by Stryker. It received FDA 510(k) clearance on 2017-11-20 under approval number K172921. 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 Stryker Self-Punching ICONIX?

Stryker Self-Punching ICONIX is a medical device that received FDA 510(k) clearance on 2017-11-20. It is manufactured by Stryker. The 510(k) number is K172921.

When was Stryker Self-Punching ICONIX approved by the FDA?

Stryker Self-Punching ICONIX received FDA 510(k) clearance on 2017-11-20, under approval number K172921.

What company makes Stryker Self-Punching ICONIX?

Stryker Self-Punching ICONIX is manufactured by Stryker.

What is the FDA product code for Stryker Self-Punching ICONIX?

The FDA product code for Stryker Self-Punching ICONIX is MBI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.