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FDA 510(k)

QUATTRO GL SUTURE ANCHOR

K-Number: K131325 · 2013-08-16

ApplicantCayenne Medical, Inc.
Decision Date2013-08-16
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

QUATTRO GL SUTURE ANCHOR is the device name listed in this FDA 510(k) record. The listed applicant is Cayenne Medical, Inc.. It received FDA 510(k) clearance on 2013-08-16 under 510(k) number K131325. 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 QUATTRO GL SUTURE ANCHOR?

QUATTRO GL SUTURE ANCHOR is a medical device that received FDA 510(k) clearance on 2013-08-16. The listed applicant is Cayenne Medical, Inc.. The 510(k) number is K131325.

When did QUATTRO GL SUTURE ANCHOR receive FDA 510(k) clearance?

QUATTRO GL SUTURE ANCHOR received FDA 510(k) clearance on 2013-08-16, under 510(k) number K131325.

Who is the listed applicant for QUATTRO GL SUTURE ANCHOR?

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

What is the FDA product code for QUATTRO GL SUTURE ANCHOR?

The FDA product code for QUATTRO GL SUTURE ANCHOR is MBI.

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Other records listing Cayenne Medical, 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.

K180274Ventix Link Knotless Anchor with InserterK172186BioWick X Implant with DriverK161033AFX™ Femoral Implant With InserterK132867SURELOCK ALL-SUTURE ANCHOR WITH INSERTER, 1.4MM, SURELOCK ALL-SUTURE ANCHOR WITH INSERTER, 2.2MMK122314QUATRO LINK KNOTLESS ANCHOR WITH INSERTER, 2.9MM-PEEK ONLYK122463APERFIX AM FEMORAL IMPLANT WITH INSERTER, 9X24 APERFIX AM FEMORAL IMPLANT WITH INSERTER, 10X24 APERFIX FEMORAL IMPLANT W

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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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