Stryker Orthopaedics Hip Systems Labeling Update
K-Number: K240418 · 2024-04-12
Decision Date2024-04-12
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Stryker Orthopaedics Hip Systems Labeling Update is a medical device manufactured by Howmedica Osteonics Corp., Dba Stryker Orthopaedics. It received FDA 510(k) clearance on 2024-04-12 under approval number K240418. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Stryker Orthopaedics Hip Systems Labeling Update?
Stryker Orthopaedics Hip Systems Labeling Update is a medical device that received FDA 510(k) clearance on 2024-04-12. It is manufactured by Howmedica Osteonics Corp., Dba Stryker Orthopaedics. The 510(k) number is K240418.
When was Stryker Orthopaedics Hip Systems Labeling Update approved by the FDA?
Stryker Orthopaedics Hip Systems Labeling Update received FDA 510(k) clearance on 2024-04-12, under approval number K240418.
What company makes Stryker Orthopaedics Hip Systems Labeling Update?
Stryker Orthopaedics Hip Systems Labeling Update is manufactured by Howmedica Osteonics Corp., Dba Stryker Orthopaedics.
What is the FDA product code for Stryker Orthopaedics Hip Systems Labeling Update?
The FDA product code for Stryker Orthopaedics Hip Systems Labeling Update is JDI.
Other Devices by Howmedica Osteonics Corp., Dba Stryker Orthopaedics
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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.