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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 a medical device manufactured by Valeris Medical. It received FDA 510(k) clearance on 2020-03-11 under approval 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. It is manufactured by Valeris Medical. The 510(k) number is K192810.

When was Apollo Suture Anchor System approved by the FDA?

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

What company makes Apollo Suture Anchor System?

Apollo Suture Anchor System is manufactured by Valeris Medical.

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

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

Related Clinical Trials

NCT07276815 OverStitch NXT Endoscopic Suture System NOT_YET_RECRUITING NCT07489820 Evaluation of the Efficacy of Negative Pressure Wound Therapy on Perineal Healing Following Abdominoperineal Amputation NOT_YET_RECRUITING NCT07581977 A Novel Two-Tooth Clip for ESD and EFTR of GIST RECRUITING NCT07587593 The IVCare Adaptive Platform Trial NOT_YET_RECRUITING NCT07554976 Suture-Mediated Closure System Following Percutaneous Common Femoral Vein Procedures RECRUITING NCT05308706 Efficacy of the Apollo System for Children With ADHD ACTIVE_NOT_RECRUITING

Related Devices (Code: MBI)

K163034SUTUREFIX Curved Suture AnchorSmith and Nephew, Inc. K162198GFS UltimateParcus Medical, LLC K162386KATOR Suture AnchorKator, LLC K161033AFX™ Femoral Implant With InserterCayenne Medical, Inc. K160996Dunamis Suture Anchor PEEK 3.0mm, 3.5mm, 4.5mm, 5.5mm, 6.5mmDunamis, LLC K161001MILAGRO ADVANCE PEEK Interference ScrewMedos International SARL

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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