510(k) K230316

Device
FlexBand; FlexPatch; FlexBand Plus
Applicant
International Life Sciences
510(k) number
K230316
Product code
OWW
Decision
Substantially Equivalent (SESE)
Decision date
2023-05-26
Date received
2023-02-06
Regulation
878.3300
Classification name
Mesh, Surgical, Absorbable, Orthopaedics, Reinforcement Of Tendon
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Tiffini Wittwer
Address
2150 Northwest Pkwy. SE Suite G Marietta GA US 30076 30076

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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K242187BioBrace®Conmed Corporation2024-11-27
K241906BioBrace® Reinforced ImplantConmed Corporation2024-07-29
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K222220SpinMedix Absorbable Fibrous MembraneCelestray Biotech Company, LLC.,2023-07-06
K203267The BioBrace ImplantBiorez, Inc.2021-04-30
K160364VersaWrap Tendon ProtectorAlafair Biosciences, Inc.2016-06-10
K121216STR GRAFTSoft Tissue Regeneration, Inc.2012-11-21