Identity
- Trade Name
- DVR® CROSSLOCKVOLAR RIM PLATE FDA UDI
- Generic Name
- Orthopaedic fixation plate, non-bioabsorbable FDA UDI
- Model / Reference
- 131824051 FDA UDI
Identifiers
- Catalog Number
- 131824051 FDA UDI
- Primary DI / UDI-DI
- 00880304814806 FDA UDI
- 510(k) Number
- K132704 FDA UDI
- FDA Product Code
- LXT FDA UDI
- GMDN Term
- Orthopaedic fixation plate, non-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
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 fixation plate, non-bioabsorbable
Dvr® Crosslockvolar Rim Plate by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Orthopaedic fixation plate, non-bioabsorbable.
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Cleared under the same submission
K132704 also covers:
- DVR® CROSSLOCK — Biomet Orthopedics, Inc.
- DVR® CROSSLOCK — Biomet Orthopedics, Inc.
- DVR® CROSSLOCK — Biomet Orthopedics, Inc.
- DVR® CROSSLOCK — Biomet Orthopedics, Inc.
- DVR® CROSSLOCKVOLAR RIM PLATE — Biomet Orthopedics, Inc.
- DVR® CROSSLOCKVOLAR RIM PLATE LEFT — Biomet Orthopedics, Inc.
- DVR® CROSSLOCKVOLAR RIM PLATE NARROW LEFT — Biomet Orthopedics, Inc.
- DVR® CROSSLOCKVOLAR RIM PLATE NARROW LEFT — Biomet Orthopedics, Inc.
- DVR® CROSSLOCKVOLAR RIM PLATE NARROW RIGHT — Biomet Orthopedics, Inc.
- DVR® CROSSLOCKVOLAR RIM PLATE NARROW RIGHT — Biomet Orthopedics, Inc.
- DVR® CROSSLOCKVOLAR RIM PLATE RIGHT — 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 071e65e5-92af-404c-82d3-2bf0818cdfa3 36 fields · synced May 30, 2026