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FDA 510(k)

KNOTLESS FIBERTAK SUTURE ANCHOR

K-Number: K130458 · 2013-05-03

ApplicantArthrex, Inc.
Decision Date2013-05-03
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KNOTLESS FIBERTAK SUTURE ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2013-05-03 under 510(k) number K130458. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KNOTLESS FIBERTAK SUTURE ANCHOR?

KNOTLESS FIBERTAK SUTURE ANCHOR is a medical device that received FDA 510(k) clearance on 2013-05-03. The listed applicant is Arthrex, Inc.. The 510(k) number is K130458.

When did KNOTLESS FIBERTAK SUTURE ANCHOR receive FDA 510(k) clearance?

KNOTLESS FIBERTAK SUTURE ANCHOR received FDA 510(k) clearance on 2013-05-03, under 510(k) number K130458.

Who is the listed applicant for KNOTLESS FIBERTAK SUTURE ANCHOR?

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 KNOTLESS FIBERTAK SUTURE ANCHOR?

The FDA product code for KNOTLESS FIBERTAK SUTURE ANCHOR is MBI.

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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.

K262975Arthrex Beaming SystemK262618Arthrex Spine Compression FT ScrewK262451Arthrex DynaNite StaplesK262357Arthrex Bioabsorbable PushLock Suture AnchorsK260624Arthrex Radial Head Replacement SystemK260018Arthrex FiberButton

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Related Devices (Code: MBI)

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.

K261869Integrity Retractable Implant Inserter (6000127)Anika Therapeutics, Inc.K262809ArthroTAK Tendon Anchor KitArthroTAK, LLCK253065Aevumed SUPERCYNCH™ Button SystemAevumed, Inc.K262677Iconix Knotless TRiverpoint MedicalK262047Grappler Suture Anchor SystemParagon 28, Inc.K262369AIR+ All-Inside Meniscal Repair Device, Curved Up;AIR+ All-Inside Meniscal Repair Device, Curved DownStryker Endoscopy

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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