SnugFit All-Suture Anchor extension
K-Number: K230544 · 2023-04-17
Device Summary
Frequently Asked Questions
What is the SnugFit All-Suture Anchor extension?
SnugFit All-Suture Anchor extension is a medical device that received FDA 510(k) clearance on 2023-04-17. The listed applicant is Medacta International S.A.. The 510(k) number is K230544.
When did SnugFit All-Suture Anchor extension receive FDA 510(k) clearance?
SnugFit All-Suture Anchor extension received FDA 510(k) clearance on 2023-04-17, under 510(k) number K230544.
Who is the listed applicant for SnugFit All-Suture Anchor extension?
The FDA 510(k) record lists Medacta International S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SnugFit All-Suture Anchor extension?
The FDA product code for SnugFit All-Suture Anchor extension is MBI.
Other records listing Medacta International S.A. 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.
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.
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.