Cemented Round Patella with JRNY Pegs
K-Number: K221939 · 2022-07-26
ApplicantSmith & Nephew, Inc.
Decision Date2022-07-26
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Cemented Round Patella with JRNY Pegs is a medical device manufactured by Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2022-07-26 under approval number K221939. 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 Cemented Round Patella with JRNY Pegs?
Cemented Round Patella with JRNY Pegs is a medical device that received FDA 510(k) clearance on 2022-07-26. It is manufactured by Smith & Nephew, Inc.. The 510(k) number is K221939.
When was Cemented Round Patella with JRNY Pegs approved by the FDA?
Cemented Round Patella with JRNY Pegs received FDA 510(k) clearance on 2022-07-26, under approval number K221939.
What company makes Cemented Round Patella with JRNY Pegs?
Cemented Round Patella with JRNY Pegs is manufactured by Smith & Nephew, Inc..
What is the FDA product code for Cemented Round Patella with JRNY Pegs?
The FDA product code for Cemented Round Patella with JRNY Pegs 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.