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Artelon receives FDA 510(k) clearance of ligament reinforcement system

Artelon Inc. has announced FDA 510(k) clearance of its FlexBand, FlexPatch and FlexBand Plus for reinforcement during ligament repair surgery, according to a press release.The FDA clearance expands the indications for the FlexBand, FlexPatch and FlexBand Plus to include medial, lateral and ulnar collateral ligaments, spring ligaments, deltoid ligaments and extra-articular ligaments, according to

Artelon, Inc s FlexBand®, FlexPatch®, and FlexBand Plus® earn FDA Clearance for Ligament Reinforcement

/PRNewswire/ Artelon Inc., announced today U.S. FDA 510(k) clearance of FlexBand®, FlexPatch®, and FlexBand Plus® for ligament repair surgery in addition to.

Artelon, Inc s  FlexBand®, FlexPatch®, And FlexBand Plus® Earn FDA Clearance For Ligament Reinforcement

Artelon, Inc s  FlexBand®, FlexPatch®, And FlexBand Plus® Earn FDA Clearance For Ligament Reinforcement
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Artelon, Inc s FlexBand®, FlexPatch®, and FlexBand Plus® earn FDA Clearance for Ligament Reinforcement

Artelon, Inc s FlexBand®, FlexPatch®, and FlexBand Plus® earn FDA Clearance for Ligament Reinforcement
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Artelon, Inc Secures $20M In Funding To Advance Surgical Treatment Of Joint Instability

Artelon, Inc Secures $20M In Funding To Advance Surgical Treatment Of Joint Instability
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