Identity
- Trade Name
- Fixone Hybrid Anchor FDA UDI
- Generic Name
- Tendon/ligament bone anchor, bioabsorbable FDA UDI
- Device Name
- The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. The anchor is manufactured from biodegradable materials (PLGA copolymer and beta-TCP) and nonabsorbable PEEK tip. A nonabsorbable suture manufactured from cobraided UHMWPE only or UHMWPE and PET fibers is inserted into the anchor. The anchor is implanted using a provided driver. FDA UDI
- Model / Reference
- KAP-55001ca FDA UDI
- Description
- The Fixone Hybrid Knotless Anchor is intended for reattaching soft tissue to bone with sutures. The anchor is manufactured from biodegradable materials (PLGA copolymer and beta-TCP) and nonabsorbable PEEK tip. A nonabsorbable suture manufactured from cobraided UHMWPE only or UHMWPE and PET fibers is inserted into the anchor. The anchor is implanted using a provided driver. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800039100601 FDA UDI
- 510(k) Number
- K203523 FDA UDI
- FDA Product Code
- MAI FDA UDI
- GMDN Term
- Tendon/ligament bone anchor, bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Tendon/ligament bone anchor, bioabsorbable
Fixone Hybrid Anchor by Aju Pharm. Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Tendon/ligament bone anchor, bioabsorbable.
- Arthrex® — Arthrex, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- HEALIX PEEK ORTHOCORD — Medos International Sàrl · Class II
- Arthrex® — Arthrex, Inc. · Class II
- 5 x 15mm CitreLock Implant — ACUITIVE TECHNOLOGIES · Class II
- Fix2Lock — OSTEONIC CO., Ltd. · Class II
- RIGIDFIX BIOCRYL — Medos International Sàrl · Class II
- Arthrex® — Arthrex, Inc. · Class II
Cleared under the same submission
K203523 also covers:
- Fixone Hybrid Anchor — AJU PHARM. CO., LTD.
- Fixone Hybrid Anchor — AJU PHARM. CO., LTD.
- Fixone Hybrid Anchor — AJU PHARM. CO., LTD.
- Fixone Hybrid Anchor — AJU PHARM. CO., LTD.
- Fixone Hybrid Anchor — AJU PHARM. CO., LTD.
- AlternatiV+ Max Knotless Anchor — GENESIS BIOLOGICS, INC.
- GENESIS HYBRID KNOTLESS DUAL THREAD ANCHOR — GENESIS BIOLOGICS, INC.
- GENESIS HYBRID KNOTLESS DUAL THREAD ANCHOR — GENESIS BIOLOGICS, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Aju Pharm. Co., Ltd.
Sources (1)
- FDA UDI 73dce3da-679f-4572-95a7-c22622458097 34 fields · synced May 30, 2026