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FDA 510(k)

SF Push- in Anchor

K-Number: K240288 · 2024-04-01

ApplicantSurgical Fusion Technologies GmbH
Decision Date2024-04-01
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SF Push- in Anchor is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Fusion Technologies GmbH. It received FDA 510(k) clearance on 2024-04-01 under 510(k) number K240288. 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 SF Push- in Anchor?

SF Push- in Anchor is a medical device that received FDA 510(k) clearance on 2024-04-01. The listed applicant is Surgical Fusion Technologies GmbH. The 510(k) number is K240288.

When did SF Push- in Anchor receive FDA 510(k) clearance?

SF Push- in Anchor received FDA 510(k) clearance on 2024-04-01, under 510(k) number K240288.

Who is the listed applicant for SF Push- in Anchor?

The FDA 510(k) record lists Surgical Fusion Technologies GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SF Push- in Anchor?

The FDA product code for SF Push- in Anchor is MAI.

Other records listing Surgical Fusion Technologies GmbH 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.

K260294SF Push-in Anchor

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.

K262357Arthrex Bioabsorbable PushLock Suture AnchorsArthrex, Inc.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 Corporation

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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