Identity
- Trade Name
- Phoenix Antegrade Nail System FDA UDI
- Generic Name
- Orthopaedic bone wire FDA UDI
- Model / Reference
- 14-443034 FDA UDI
Identifiers
- Catalog Number
- 14-443034 FDA UDI
- Primary DI / UDI-DI
- 00887868096181 FDA UDI
- 510(k) Number
- K072161 FDA UDI
- FDA Product Code
- HSB FDA UDI
- GMDN Term
- Orthopaedic bone wire FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3020 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
Category: Orthopaedic bone wire
Phoenix Antegrade Nail System by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Orthopaedic bone wire.
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Cleared under the same submission
K072161 also covers:
- PHOENIX ANTEGRADE NAIL SYSTEM — Biomet Orthopedics, Inc.
- PHOENIX ANTEGRADE NAIL SYSTEM — Biomet Orthopedics, Inc.
- PHOENIX ANTEGRADE NAIL SYSTEM — Biomet Orthopedics, Inc.
- PHOENIX ANTEGRADE NAIL SYSTEM — Biomet Orthopedics, Inc.
- PHOENIX ANTEGRADE NAIL SYSTEM — Biomet Orthopedics, Inc.
- PHOENIX ANTEGRADE NAIL SYSTEM — Biomet Orthopedics, Inc.
- PHOENIX ANTEGRADE NAIL SYSTEM — Biomet Orthopedics, Inc.
- PHOENIX ANTEGRADE NAIL SYSTEM — Biomet Orthopedics, Inc.
- PHOENIX ANTEGRADE NAIL SYSTEM — Biomet Orthopedics, Inc.
- PHOENIX NAIL SYSTEM — Biomet Orthopedics, Inc.
- PHOENIX NAIL SYSTEM — Biomet Orthopedics, Inc.
- PHOENIX NAIL SYSTEM — 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 |
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Manufacturer
- Manufacturer
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI 238c21ae-683e-4061-923b-fd0673a87156 36 fields · synced Jun 6, 2026