ProZip Knotless Implant
K-Number: K253024 · 2025-10-16
ApplicantRiverpoint Medical
Decision Date2025-10-16
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
ProZip Knotless Implant is a medical device manufactured by Riverpoint Medical. It received FDA 510(k) clearance on 2025-10-16 under approval number K253024. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ProZip Knotless Implant?
ProZip Knotless Implant is a medical device that received FDA 510(k) clearance on 2025-10-16. It is manufactured by Riverpoint Medical. The 510(k) number is K253024.
When was ProZip Knotless Implant approved by the FDA?
ProZip Knotless Implant received FDA 510(k) clearance on 2025-10-16, under approval number K253024.
What company makes ProZip Knotless Implant?
ProZip Knotless Implant is manufactured by Riverpoint Medical.
What is the FDA product code for ProZip Knotless Implant?
The FDA product code for ProZip Knotless Implant is GAT.
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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.