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FDA 510(k)

DYNATAPE Suture

K-Number: K203186 · 2021-03-18

ApplicantMedos International SARL
Decision Date2021-03-18
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DYNATAPE Suture is a medical device manufactured by Medos International SARL. It received FDA 510(k) clearance on 2021-03-18 under approval number K203186. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNATAPE Suture?

DYNATAPE Suture is a medical device that received FDA 510(k) clearance on 2021-03-18. It is manufactured by Medos International SARL. The 510(k) number is K203186.

When was DYNATAPE Suture approved by the FDA?

DYNATAPE Suture received FDA 510(k) clearance on 2021-03-18, under approval number K203186.

What company makes DYNATAPE Suture?

DYNATAPE Suture is manufactured by Medos International SARL.

What is the FDA product code for DYNATAPE Suture?

The FDA product code for DYNATAPE Suture is GAT.

Other Devices by Medos International SARL

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Related Devices (Code: GAT)

K160854MaxBraid BroadBand Suture and Expressbraid BroadBand Graft Manipulation SutureBiomet Manafacturing Corp. K162247PERMATAPEMedos International SARL K162310XBraid TT Suture TapeStryker K161638SPEEDTRAP Graft Preparation SystemMedos International SARL K153089'cottony' II TAPE, PLEDGETSTeleflexmedical, Inc. K153087IvyAIR Meniscus System, Curved, IvyAIR Meniscus System, Straight, IvyAIR Meniscus System, Reverse CurvedIvy Sports Medicine, LLC

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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