Veritas Reverse Total Shoulder System
K-Number: K253992 · 2026-05-07
ApplicantRestor3D
Decision Date2026-05-07
Product CodePHX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Veritas Reverse Total Shoulder System is a medical device manufactured by Restor3D. It received FDA 510(k) clearance on 2026-05-07 under approval number K253992. The device is classified under product code PHX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Veritas Reverse Total Shoulder System?
Veritas Reverse Total Shoulder System is a medical device that received FDA 510(k) clearance on 2026-05-07. It is manufactured by Restor3D. The 510(k) number is K253992.
When was Veritas Reverse Total Shoulder System approved by the FDA?
Veritas Reverse Total Shoulder System received FDA 510(k) clearance on 2026-05-07, under approval number K253992.
What company makes Veritas Reverse Total Shoulder System?
Veritas Reverse Total Shoulder System is manufactured by Restor3D.
What is the FDA product code for Veritas Reverse Total Shoulder System?
The FDA product code for Veritas Reverse Total Shoulder System is PHX.
Related PubMed Literature
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.