Legion Inserts with JRNY Lock
K-Number: K220896 · 2022-04-26
ApplicantSmith & Nephew, Inc.
Decision Date2022-04-26
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Legion Inserts with JRNY Lock is a medical device manufactured by Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2022-04-26 under approval number K220896. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Legion Inserts with JRNY Lock?
Legion Inserts with JRNY Lock is a medical device that received FDA 510(k) clearance on 2022-04-26. It is manufactured by Smith & Nephew, Inc.. The 510(k) number is K220896.
When was Legion Inserts with JRNY Lock approved by the FDA?
Legion Inserts with JRNY Lock received FDA 510(k) clearance on 2022-04-26, under approval number K220896.
What company makes Legion Inserts with JRNY Lock?
Legion Inserts with JRNY Lock is manufactured by Smith & Nephew, Inc..
What is the FDA product code for Legion Inserts with JRNY Lock?
The FDA product code for Legion Inserts with JRNY Lock is JWH.
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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.