Identity
- Trade Name
- Pivot Bipolar FDA UDI
- Generic Name
- Bipolar femoral head outer component, hemiarthroplasty FDA UDI
- Device Name
- 22x42mm Bipolar FDA UDI
- Model / Reference
- 133-2242 FDA UDI
- Description
- 22x42mm Bipolar FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00822409015115 FDA UDI
- 510(k) Number
- K050966 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
Dimensions & Sizes
- Size
- Outer Diameter — 42 Millimeter FDA UDILumen/Inner Diameter — 22 Millimeter FDA UDI
Category: Bipolar femoral head outer component, hemiarthroplasty
Pivot Bipolar by Ortho Development Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bipolar femoral head outer component, hemiarthroplasty.
- 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
- United Hip System, U2 Bipolar Implant — UNITED ORTHOPEDIC CORP. · Class II
Cleared under the same submission
K050966 also covers:
- Pivot Bipolar — ORTHO DEVELOPMENT CORP.
- Pivot Bipolar — ORTHO DEVELOPMENT CORP.
- Pivot Bipolar — ORTHO DEVELOPMENT CORP.
- Pivot Bipolar — ORTHO DEVELOPMENT CORP.
- Pivot Bipolar — ORTHO DEVELOPMENT CORP.
- Pivot Bipolar — ORTHO DEVELOPMENT CORP.
- Pivot Bipolar — ORTHO DEVELOPMENT CORP.
- Pivot Bipolar — ORTHO DEVELOPMENT CORP.
- Pivot Bipolar — ORTHO DEVELOPMENT CORP.
- Pivot Bipolar — ORTHO DEVELOPMENT CORP.
- Pivot Bipolar — ORTHO DEVELOPMENT CORP.
- Pivot Bipolar — ORTHO DEVELOPMENT CORP.
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
- Ortho Development Corp.
Sources (1)
- FDA UDI c1a0340f-fb6e-4813-8ab7-51afd9250a99 36 fields · synced May 30, 2026