ClearanceBrief
510(k) K233601 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue

Fixone Meniscal Repair

ApplicantAju Pharm Co., Ltd., Seongnam, KR
DecisionSubstantially Equivalent, Aug 2, 2024
ReceivedNov 9, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233601

DateFirm and productCodeLinked 510(k)
Jan 26, 2026Aju Pharm Co., Ltd.
Fixone Hybrid Anchor
Open, Classified
MAINone listed
Jan 26, 2026Aju Pharm Co., Ltd.
Fixone Biocomposite Anchor
Open, Classified
MAINone listed
Jan 26, 2026Aju Pharm Co., Ltd.
Genesis Screw-In Anchor
Open, Classified
MAINone listed
Jan 26, 2026Aju Pharm Co., Ltd.
Genesis Dual Thread Screw-In Anchor
Open, Classified
MAINone listed
Jan 26, 2026Aju Pharm Co., Ltd.
Genesis Knotless Anchor
Open, Classified
MAINone listed
Jan 26, 2026Aju Pharm Co., Ltd.
Genesis Push-In Suture Anchor
Open, Classified
MAINone listed
Jan 26, 2026Aju Pharm Co., Ltd.
AlternatiV+ Max Knotless Anchor
Open, Classified
MAINone listed
Jan 26, 2026Aju Pharm Co., Ltd.
AlternatiV+ Screw-In Anchor
Open, Classified
MAINone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.