Bard 3DMax Mesh
K-Number: K233402 · 2023-11-01
Device Summary
Frequently Asked Questions
What is the Bard 3DMax Mesh?
Bard 3DMax Mesh is a medical device that received FDA 510(k) clearance on 2023-11-01. The listed applicant is Davol Inc., Subsidiary of C. R. Bard, Inc.. The 510(k) number is K233402.
When did Bard 3DMax Mesh receive FDA 510(k) clearance?
Bard 3DMax Mesh received FDA 510(k) clearance on 2023-11-01, under 510(k) number K233402.
Who is the listed applicant for Bard 3DMax Mesh?
The FDA 510(k) record lists Davol Inc., Subsidiary of C. R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Bard 3DMax Mesh?
The FDA product code for Bard 3DMax Mesh is FTL.
Other records listing Davol Inc., Subsidiary of C. R. Bard, 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: FTL)
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.