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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Riverpoint Medical. It received FDA 510(k) clearance on 2025-10-16 under 510(k) 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. The listed applicant is Riverpoint Medical. The 510(k) number is K253024.

When did ProZip Knotless Implant receive FDA 510(k) clearance?

ProZip Knotless Implant received FDA 510(k) clearance on 2025-10-16, under 510(k) number K253024.

Who is the listed applicant for ProZip Knotless Implant?

The FDA 510(k) record lists Riverpoint Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ProZip Knotless Implant?

The FDA product code for ProZip Knotless Implant is GAT.

Other records listing Riverpoint Medical 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.

K253693Strut Suture; No-Tie ButtonK253695LigaMendK252201HS FiberK252144Iconix Speed Anchor; Iconix Speed HA+ AnchorK243988RootMend MRRK242494OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct

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Related Devices (Code: GAT)

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.

K261021EasyWhip FamilyWinter Innovations, Inc.K260775Polyethylene;Polyethylene Fusion;Polyethylene OrthoTape™Teleflex Medical, LLCK254275HyperSuture All Green Extension LineThreadstone, LLCK254188Meniscus VersaflexGM Dos Reis Industria e Comercio Ltda.K253145Pre-Sutured TendonRti Surgical, Inc.K252225PowerKnot High Strength SuturesMedacta International S.A.

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.

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