Identity
- Trade Name
- Large QWIX FDA UDI
- Generic Name
- Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
- Device Name
- The Fixation screw is a cannulated titanium alloy screw of 5.5mm diameters partially threaded and decreased thread at the head, allowing optimal compression. The screw has a self-drilling and self-tapping screw tip. These features enable its use in totally intra-osseous fixation. The screw is cannulated in order to enable the use of a K-wire for optimal positioning. Delivered sterile. FDA UDI
- Model / Reference
- 111565SND FDA UDI
- Description
- The Fixation screw is a cannulated titanium alloy screw of 5.5mm diameters partially threaded and decreased thread at the head, allowing optimal compression. The screw has a self-drilling and self-tapping screw tip. These features enable its use in totally intra-osseous fixation. The screw is cannulated in order to enable the use of a K-wire for optimal positioning. Delivered sterile. FDA UDI
Identifiers
- Catalog Number
- 111565SND FDA UDI
- Primary DI / UDI-DI
- 10381780047100 FDA UDI
- 510(k) Number
- K050346 FDA UDI
- FDA Product Code
- HWC FDA UDI
- GMDN Term
- Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
Yes
FDA UDI
Category: Orthopaedic bone screw, non-bioabsorbable, sterile
Large QWIX by Newdeal Sas — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic bone screw, non-bioabsorbable, sterile.
- EPS Plating System Screw — GRAMERCY EXTREMITY ORTHOPEDICS, LLC. · Class II
- A.L.P.S.CORTICAL SCREW — Biomet Orthopedics, Inc. · Class II
- Peri-Loc — Smith & Nephew, Inc. · Class II
- Cortical Screw 2.5mm x 24mm Sterile — BIOPRO, INC. · Class II
- OsteoMed — Osteomed Corp. · Class II
- 3.5mm x 10mm Ti Cortical Screw — WISHBONE MEDICAL INC. · Class II
- primaLOK FF — Wenzel Spine · U
- MAX VPC™VARIABLE PITCH COMPRESSION SCREW — Biomet Orthopedics, Inc. · Class II
Cleared under the same submission
K050346 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Newdeal Sas
Sources (1)
- FDA UDI 8ebd48b9-3c8d-4e5a-ba2a-ce2b02a7886e 39 fields · synced May 31, 2026