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FDA 510(k)

SnugFit All-Suture Anchor

K-Number: K203485 · 2021-01-19

ApplicantMedacta International S.A.
Decision Date2021-01-19
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SnugFit All-Suture Anchor is a medical device manufactured by Medacta International S.A.. It received FDA 510(k) clearance on 2021-01-19 under approval number K203485. 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 SnugFit All-Suture Anchor?

SnugFit All-Suture Anchor is a medical device that received FDA 510(k) clearance on 2021-01-19. It is manufactured by Medacta International S.A.. The 510(k) number is K203485.

When was SnugFit All-Suture Anchor approved by the FDA?

SnugFit All-Suture Anchor received FDA 510(k) clearance on 2021-01-19, under approval number K203485.

What company makes SnugFit All-Suture Anchor?

SnugFit All-Suture Anchor is manufactured by Medacta International S.A..

What is the FDA product code for SnugFit All-Suture Anchor?

The FDA product code for SnugFit All-Suture Anchor is MBI.

Related PubMed Literature

PMID: 40868376 Correlation Analysis of Suture Anchor Pull-Out Strength with Cortical Bone Thickness and Cancellous Bone Density on a Finite Element Model. Bioengineering (Basel, Switzerland) (2025)

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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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