UNITRAX MODULAR UNIPOLAR SYSTEM
FDA 510(k) clearance K014226 · decided 2002-01-25
Clearance details
- K-number
- K014226
- Device name
- UNITRAX MODULAR UNIPOLAR SYSTEM
- Applicant
- Howmedica Osteonics Corp.
- Decision
- Substantially Equivalent
- Date received
- 2001-12-26
- Decision date
- 2002-01-25
- Days to decision
- 30 days
- Clearance type
- Special
- Product code
- KWL
- Device class
- 2
- Regulation number
- 888.3360
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Allendale, NJ, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Howmedica Osteonics Corp.
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| REMEDY POLY+PLUS SNAP FIT Acetabular Cup (K262290) | Osteoremedies, LLC | 2026-07-24 |
| Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone Cement (K260536) | Depuy Ireland UC | 2026-05-15 |
| OsteoRemedies Hip Spacer System (K253675) | Osteoremedies, LLC | 2025-12-23 |
| InterSpace GV Hip Spacer (K252326) | Tecres S.P.A. | 2025-08-06 |
| Synicem Hip Spacer; Synicem Knee Spacer; Synicem Shoulder Spacer (K242865) | Biocomposites, Ltd. | 2025-06-12 |
| COPAL® exchange G hip spacer; COPAL® G+V (K234028) | Heraeus Medical GmbH | 2024-02-15 |
| UHR Bipolar Implants, Restoration GAP II Implants (K222632) | Howmedica Osteonics Corp., Dba Stryker Orthopaedics | 2022-10-21 |
| OsteoRemedies Hip Spacer System (K192995) | Osteoremedies, LLC | 2020-01-10 |
| REMEDY Acetabular Cup (K191981) | Osteoremedies, LLC | 2019-08-23 |
| REMEDY PLUS Hip Spacer, UNITE PLUS Bone Cement (K172906) | Osteoremedies, LLC | 2018-08-29 |
| Remedy Acetabular Cup (K173967) | Osteoremedies, LLC | 2018-02-22 |
| Evolve UniPolar Head (K143184) | Signature Orthopaedics Pty, Ltd. | 2015-03-17 |
Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in partial hip ar recall (Z-2370-2024) | Howmedica Osteonics Corp. | 2024-07-16 |
| UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in partial hip ar recall (Z-2371-2024) | Howmedica Osteonics Corp. | 2024-07-16 |
| UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in partial hip ar recall (Z-2372-2024) | Howmedica Osteonics Corp. | 2024-07-16 |
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| Trident Alumina Insert (625-0T-XXX); Osteonics® ABC/Trident® System (P000013/S027) | Howmedica Osteonics Corp. | 2025-09-17 |
| Trident Acetabular System: Trident Alumina Inserts (P000013/S026) | Howmedica Osteonics Corp. | 2025-05-23 |
| Trident® Acetabular System (P000013/S025) | Howmedica Osteonics Corp. | 2024-03-08 |
| Trident(R), ABC(R) (P000013/S024) | Howmedica Osteonics Corp. | 2024-01-23 |
| Trident Ceramic System (P000013/S021) | Howmedica Osteonics Corp. | 2023-12-20 |
| Trident(R), ABC(R) (P000013/S023) | Howmedica Osteonics Corp. | 2023-12-19 |
| Trident®, ABC® (P000013/S022) | Howmedica Osteonics Corp. | 2023-09-27 |
| Trident Acetabular System: Trident Alumina Inserts (P000013/S020) | Howmedica Osteonics Corp. | 2022-04-01 |