Identity
- Trade Name
- CANNULATED SCREW 4.0MM X 22MM (PARTIAL THREAD) FDA UDI
- Generic Name
- Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
- Model / Reference
- 110009808 FDA UDI
Identifiers
- Catalog Number
- 110009808 FDA UDI
- Primary DI / UDI-DI
- 00887868110153 FDA UDI
- 510(k) Number
- K140891 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
No
FDA UDI
MR Conditional FDA UDI
Category: Orthopaedic bone screw, non-bioabsorbable, sterile
Cannulated Screw 4.0mm X 22mm (partial Thread) by Biomet Orthopedics, Inc. — 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
- 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
- Libertas — MAXX ORTHOPEDICS INC. · Class II
- Exactech — Exactech, Inc. · Class II
Cleared under the same submission
K140891 also covers:
- Biomet Cannulated Screw System — Biomet Orthopedics, Inc.
- CANNULATED SCREW 4.0MM X 10MM (FULL THREAD) — Biomet Orthopedics, Inc.
- CANNULATED SCREW 4.0MM X 16MM (PARTIAL THREAD) — Biomet Orthopedics, Inc.
- CANNULATED SCREW 4.0MM X 50MM (PARTIAL THREAD) — Biomet Orthopedics, Inc.
- CANNULATED SCREW 4.0MM X 55MM (FULL THREAD) — Biomet Orthopedics, Inc.
- CANNULATED SCREW 4.0MM X 65MM (FULL THREAD) — Biomet Orthopedics, Inc.
- CANNULATED SCREW 4.0MM X 70MM (PARTIAL THREAD) — Biomet Orthopedics, Inc.
- CANNULATED SCREW 5.0MM X 34MM (FULL THREAD) — Biomet Orthopedics, Inc.
- CANNULATED SCREW 5.0MM X 34MM (FULL THREAD) — Biomet Orthopedics, Inc.
- CANNULATED SCREW 5.0MM X 44MM (FULL THREAD) — Biomet Orthopedics, Inc.
- CANNULATED SCREW 5.0MM X 95MM (FULL THREAD) — Biomet Orthopedics, Inc.
- CANNULATED SCREW 5.0MM X 95MM (FULL THREAD) — Biomet Orthopedics, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI 6b229c7c-d131-45ff-8792-bd8db2fb87e2 36 fields · synced May 30, 2026