Smith & Nephew Hip Systems
K-Number: K211176 · 2022-07-01
ApplicantSmith & Nephew, Inc.
Decision Date2022-07-01
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Smith & Nephew Hip Systems is a medical device manufactured by Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2022-07-01 under approval number K211176. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Smith & Nephew Hip Systems?
Smith & Nephew Hip Systems is a medical device that received FDA 510(k) clearance on 2022-07-01. It is manufactured by Smith & Nephew, Inc.. The 510(k) number is K211176.
When was Smith & Nephew Hip Systems approved by the FDA?
Smith & Nephew Hip Systems received FDA 510(k) clearance on 2022-07-01, under approval number K211176.
What company makes Smith & Nephew Hip Systems?
Smith & Nephew Hip Systems is manufactured by Smith & Nephew, Inc..
What is the FDA product code for Smith & Nephew Hip Systems?
The FDA product code for Smith & Nephew Hip Systems is LPH.
Related Clinical Trials
Other Devices by Smith & Nephew, Inc.
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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.