AEVUMED PHANTOM Suture Anchors
K-Number: K180464 · 2018-05-31
Device Summary
Frequently Asked Questions
What is the AEVUMED PHANTOM Suture Anchors?
AEVUMED PHANTOM Suture Anchors is a medical device that received FDA 510(k) clearance on 2018-05-31. The listed applicant is Aevumed, Inc.. The 510(k) number is K180464.
When did AEVUMED PHANTOM Suture Anchors receive FDA 510(k) clearance?
AEVUMED PHANTOM Suture Anchors received FDA 510(k) clearance on 2018-05-31, under 510(k) number K180464.
Who is the listed applicant for AEVUMED PHANTOM Suture Anchors?
The FDA 510(k) record lists Aevumed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AEVUMED PHANTOM Suture Anchors?
The FDA product code for AEVUMED PHANTOM Suture Anchors is MBI.
Other records listing Aevumed, Inc. 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.