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FDA 510(k)

Apollo Suture Anchor System

K-Number: K192810 · 2020-03-11

ApplicantValeris Medical
Decision Date2020-03-11
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Apollo Suture Anchor System is the device name listed in this FDA 510(k) record. The listed applicant is Valeris Medical. It received FDA 510(k) clearance on 2020-03-11 under 510(k) number K192810. 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 Apollo Suture Anchor System?

Apollo Suture Anchor System is a medical device that received FDA 510(k) clearance on 2020-03-11. The listed applicant is Valeris Medical. The 510(k) number is K192810.

When did Apollo Suture Anchor System receive FDA 510(k) clearance?

Apollo Suture Anchor System received FDA 510(k) clearance on 2020-03-11, under 510(k) number K192810.

Who is the listed applicant for Apollo Suture Anchor System?

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

What is the FDA product code for Apollo Suture Anchor System?

The FDA product code for Apollo Suture Anchor System is MBI.

Other records listing Valeris 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.

K193108Bonecam Suture Anchor

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.

K262047Grappler Suture Anchor SystemParagon 28, Inc.K262369AIR+ All-Inside Meniscal Repair Device, Curved Up;AIR+ All-Inside Meniscal Repair Device, Curved DownStryker EndoscopyK261770Suture Button Repair SystemSkeletal Dynamics, Inc.K261632Thunderbolt SystemResponsive Arthroscopy, Inc.K261968Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one black knotless and one blue MINITAPE suture (72205981); Q-FIX KNOTLESS All-Suture Anchor, 2.8mm, with one blue knotless and one black MINITAPE suture (72205982)Smith & Nephew, Inc.K260018Arthrex FiberButtonArthrex, Inc.

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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