Identity
- Trade Name
- BONE SCREW, CORTICAL FDA UDI
- Generic Name
- Orthopaedic bone screw, non-bioabsorbable, non-sterile FDA UDI
- Model / Reference
- 14022-100 FDA UDI
Identifiers
- Catalog Number
- 14022100 FDA UDI
- Primary DI / UDI-DI
- 00887868009990 FDA UDI
- FDA Product Code
- HRS FDA UDIHSB FDA UDIJEC FDA UDI
- GMDN Term
- Orthopaedic bone screw, non-bioabsorbable, non-sterile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 FDA UDI888.3020 FDA UDI888.3040 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic bone screw, non-bioabsorbable, non-sterile
Bone Screw, Cortical by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K833865 also covers:
- ACTIVE COMPRESSION PLATE — Biomet Orthopedics, Inc.
- ACTIVE COMPRESSION PLATE — Biomet Orthopedics, Inc.
- ACTIVE COMPRESSION PLATE — Biomet Orthopedics, Inc.
- ACTIVE COMPRESSION PLATE — Biomet Orthopedics, Inc.
- ACTIVE COMPRESSION PLATE — Biomet Orthopedics, Inc.
- BONE SCREW, CORTICAL — Biomet Orthopedics, Inc.
- BONE SCREW, CORTICAL — Biomet Orthopedics, Inc.
- BONE SCREW, CORTICAL — Biomet Orthopedics, Inc.
- BONE SCREW, CORTICAL — Biomet Orthopedics, Inc.
- BONE SCREW, CORTICAL — Biomet Orthopedics, Inc.
- BONE SCREW, CORTICAL — Biomet Orthopedics, Inc.
- BONE SCREW, CORTICAL — Biomet Orthopedics, Inc.
K871539 also covers:
- A.R.T.™FEMORAL NAIL — Biomet Orthopedics, Inc.
- A.R.T.™FEMORAL NAIL — Biomet Orthopedics, Inc.
- A.R.T.™FEMORAL NAIL — Biomet Orthopedics, Inc.
- A.R.T.™FEMORAL NAIL — Biomet Orthopedics, Inc.
- A.R.T.™FEMORAL NAIL — Biomet Orthopedics, Inc.
- A.R.T.™FEMORAL NAIL — Biomet Orthopedics, Inc.
- A.R.T.™FEMORAL NAIL — Biomet Orthopedics, Inc.
- A.R.T.™FEMORAL NAIL — Biomet Orthopedics, Inc.
- A.R.T.™FEMORAL NAIL — Biomet Orthopedics, Inc.
- A.R.T.™FEMORAL NAIL — Biomet Orthopedics, Inc.
- A.R.T.™FEMORAL NAIL — Biomet Orthopedics, Inc.
- A.R.T.™FEMORAL NAIL — 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 dec01f42-ed69-4606-a8ca-8d881b7e77b1 36 fields · synced May 30, 2026