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FDA 510(k)

PERMALOOP Suture, PERMATAPE Suture

K-Number: K220219 · 2022-04-26

ApplicantMedos International SARL
Decision Date2022-04-26
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PERMALOOP Suture, PERMATAPE Suture is a medical device manufactured by Medos International SARL. It received FDA 510(k) clearance on 2022-04-26 under approval number K220219. 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 PERMALOOP Suture, PERMATAPE Suture?

PERMALOOP Suture, PERMATAPE Suture is a medical device that received FDA 510(k) clearance on 2022-04-26. It is manufactured by Medos International SARL. The 510(k) number is K220219.

When was PERMALOOP Suture, PERMATAPE Suture approved by the FDA?

PERMALOOP Suture, PERMATAPE Suture received FDA 510(k) clearance on 2022-04-26, under approval number K220219.

What company makes PERMALOOP Suture, PERMATAPE Suture?

PERMALOOP Suture, PERMATAPE Suture is manufactured by Medos International SARL.

What is the FDA product code for PERMALOOP Suture, PERMATAPE Suture?

The FDA product code for PERMALOOP Suture, PERMATAPE Suture is GAT.

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Related Devices (Code: GAT)

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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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