EVOS Wrist Spanning Plate
K-Number: K213123 · 2022-10-18
ApplicantSmith & Nephew, Inc.
Decision Date2022-10-18
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
EVOS Wrist Spanning Plate is a medical device manufactured by Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2022-10-18 under approval number K213123. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the EVOS Wrist Spanning Plate?
EVOS Wrist Spanning Plate is a medical device that received FDA 510(k) clearance on 2022-10-18. It is manufactured by Smith & Nephew, Inc.. The 510(k) number is K213123.
When was EVOS Wrist Spanning Plate approved by the FDA?
EVOS Wrist Spanning Plate received FDA 510(k) clearance on 2022-10-18, under approval number K213123.
What company makes EVOS Wrist Spanning Plate?
EVOS Wrist Spanning Plate is manufactured by Smith & Nephew, Inc..
What is the FDA product code for EVOS Wrist Spanning Plate?
The FDA product code for EVOS Wrist Spanning Plate is HRS.
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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.