Bard 3DMax Mesh
K-Number: K233402 · 2023-11-01
Decision Date2023-11-01
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Bard 3DMax Mesh is a medical device manufactured by Davol Inc., Subsidiary of C. R. Bard, Inc.. It received FDA 510(k) clearance on 2023-11-01 under approval number K233402. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Davol Inc., Subsidiary of C. R. Bard, Inc.. The 510(k) number is K233402.
When was Bard 3DMax Mesh approved by the FDA?
Bard 3DMax Mesh received FDA 510(k) clearance on 2023-11-01, under approval number K233402.
What company makes Bard 3DMax Mesh?
Bard 3DMax Mesh is manufactured by Davol Inc., Subsidiary of C. R. Bard, Inc..
What is the FDA product code for Bard 3DMax Mesh?
The FDA product code for Bard 3DMax Mesh is FTL.
Other Devices by Davol Inc., Subsidiary of C. R. Bard, Inc.
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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.