28mm/38D MDM X3 Insert for MDM Liner
K-Number: K233724 · 2024-03-11
Device Summary
Frequently Asked Questions
What is the 28mm/38D MDM X3 Insert for MDM Liner?
28mm/38D MDM X3 Insert for MDM Liner is a medical device that received FDA 510(k) clearance on 2024-03-11. The listed applicant is Howmedica Osteonics Corp., Dba Stryker Orthopaedics. The 510(k) number is K233724.
When did 28mm/38D MDM X3 Insert for MDM Liner receive FDA 510(k) clearance?
28mm/38D MDM X3 Insert for MDM Liner received FDA 510(k) clearance on 2024-03-11, under 510(k) number K233724.
Who is the listed applicant for 28mm/38D MDM X3 Insert for MDM Liner?
The FDA 510(k) record lists Howmedica Osteonics Corp., Dba Stryker Orthopaedics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 28mm/38D MDM X3 Insert for MDM Liner?
The FDA product code for 28mm/38D MDM X3 Insert for MDM Liner is LZO.
Other records listing Howmedica Osteonics Corp., Dba Stryker Orthopaedics as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LZO)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.