Identity
- Trade Name
- SELF CENTERING FDA UDI
- Generic Name
- Bipolar femoral head outer component, hemiarthroplasty FDA UDI
- Device Name
- SELF CENTERING BI-POLAR HEAD 22.225mm ID 55mm OD FDA UDI
- Model / Reference
- 1037-55-000 FDA UDI
- Description
- SELF CENTERING BI-POLAR HEAD 22.225mm ID 55mm OD FDA UDI
Identifiers
- Catalog Number
- 103755000 FDA UDI
- Primary DI / UDI-DI
- 10603295003687 FDA UDI
- 510(k) Number
- K812672 FDA UDI
- FDA Product Code
- KWY FDA UDI
- GMDN Term
- Bipolar femoral head outer component, hemiarthroplasty FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3390 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: Bipolar femoral head outer component, hemiarthroplasty
Self Centering by Depuy Orthopaedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bipolar femoral head outer component, hemiarthroplasty.
- Pivot Bipolar — ORTHO DEVELOPMENT CORP. · Class II
- BIO-MOORE ENDO II HIP SYSTEM — Biomet Orthopedics, Inc. · Class II
- TANDEM — Smith & Nephew, Inc. · Class II
- Consensus Hip System — SHALBY ADVANCED TECHNOLOGIES, INC. · Class II
- Endohead — Medacta International · Class II
- UHR — Howmedica Osteonics Corp. · Class II
- SLR BIPOLAR — MicroPort Orthopedics Inc. · Class II
- MultiPolar® — Zimmer, Inc. · Class II
Cleared under the same submission
K812672 also covers:
- SELF CENTERING — DEPUY ORTHOPAEDICS, INC.
- SELF CENTERING — DEPUY ORTHOPAEDICS, INC.
- SELF CENTERING — DEPUY ORTHOPAEDICS, INC.
- SELF CENTERING — DEPUY ORTHOPAEDICS, INC.
- SELF CENTERING — DEPUY ORTHOPAEDICS, INC.
- SELF CENTERING — DEPUY ORTHOPAEDICS, INC.
- SELF CENTERING — DEPUY ORTHOPAEDICS, INC.
- SELF CENTERING — DEPUY ORTHOPAEDICS, INC.
- SELF CENTERING — DEPUY ORTHOPAEDICS, INC.
- SELF CENTERING — DEPUY ORTHOPAEDICS, INC.
- SELF CENTERING — DEPUY ORTHOPAEDICS, INC.
- SELF CENTERING — DEPUY ORTHOPAEDICS, 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
- Depuy Orthopaedics, Inc.
Sources (1)
- FDA UDI a4b867b5-8338-4142-a283-c5735e4c8b12 36 fields · synced Jun 8, 2026