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FDA 510(k)

Arthrex Bioabsorbable PushLock Suture Anchors

K-Number: K262357 · 2026-08-07

ApplicantArthrex, Inc.
Decision Date2026-08-07
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Arthrex Bioabsorbable PushLock Suture Anchors is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2026-08-07 under 510(k) number K262357. The device is classified under product code MAI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Arthrex Bioabsorbable PushLock Suture Anchors?

Arthrex Bioabsorbable PushLock Suture Anchors is a medical device that received FDA 510(k) clearance on 2026-08-07. The listed applicant is Arthrex, Inc.. The 510(k) number is K262357.

When did Arthrex Bioabsorbable PushLock Suture Anchors receive FDA 510(k) clearance?

Arthrex Bioabsorbable PushLock Suture Anchors received FDA 510(k) clearance on 2026-08-07, under 510(k) number K262357.

Who is the listed applicant for Arthrex Bioabsorbable PushLock Suture Anchors?

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

What is the FDA product code for Arthrex Bioabsorbable PushLock Suture Anchors?

The FDA product code for Arthrex Bioabsorbable PushLock Suture Anchors is MAI.

Related Clinical Trials

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.

NCT05753891Trapeziectomy: Internal Brace vs. Ligament Reconstruction (Prospective)TERMINATEDNCT06829667Retrospective Study of Suture Tape for Soft Tissue Reconstruction in Patients Suffering From Lateral Ankle InstabilityCOMPLETED

Other records listing Arthrex, Inc. 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.

K260624Arthrex Radial Head Replacement SystemK260018Arthrex FiberButtonK260809Arthrex Sterile VAL and VAL KreuLock™ Compression Screw SystemK253931Arthrex Bioabsorbable PushLock Suture AnchorsK254215Arthrex Beaming SystemK260561Arthrex FiberTak Suture Anchor

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Related Devices (Code: MAI)

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.

K253931Arthrex Bioabsorbable PushLock Suture AnchorsArthrex, Inc.K260294SF Push-in AnchorSurgical Fusion Technologies GmbHK254055OSSIOfiber® Suture AnchorOSSIO , Ltd.K251680Biosteon® ScrewBiocomposites, Ltd.K252946BioBrace® Extra-Articular Ligament Augmentation KitConmed CorporationK252022OSSIOfiber® Interference ScrewOSSIO , Ltd.

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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