Ceramax® Ceramic Total Hip System
FDA premarket approval P070026/S116 · decided 2025-02-11
Approval details
- PMA number
- P070026
- Supplement
- S116
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Ceramax® Ceramic Total Hip System
- Generic name
- Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented
- Applicant
- DePuy Orthopaedics, Inc.
- Date received
- 2024-12-16
- Decision date
- 2025-02-11
- Days to decision
- 57 days
- Decision code
- APPR
- Product code
- MRA
- Advisory committee
- Orthopedic
- Expedited review
- No
- Location
- Warsaw, IN
- Statement
- Approval for a manufacturing site located at Johnson & Johnson Medical (DePuy Suzhou) Ltd., No. 299, Changyang Street, Suzhou Industrial Park, Suzhou, Jiangsu, China, as well as a sterilization site located at Shanghai JPY Ion-Tech. Co., Ltd, No. 1168, Huijin Rd., Qingpu Industrial Zone, Shanghai, China, to manufacture and sterilize PINNACLE® Acetabular Cups of the CERAMAX® Ceramic Total Hip System.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| DePuy ATTUNE™ Knee System (K252887) | DePuy Orthopaedics, Inc. | 2026-05-22 |
| CUPTIMIZE™ Advanced (K231503) | DePuy Orthopaedics, Inc. | 2023-08-22 |
| DePuy Corail AMT Hip Prosthesis (K213839) | DePuy Orthopaedics, Inc. | 2022-01-06 |
| DELTA XTEND Reverse Shoulder System (K210167) | DePuy Orthopaedics, Inc. | 2021-02-19 |
| DePuy Corail AMT Hip Prosthesis (K203167) | DePuy Orthopaedics, Inc. | 2020-11-19 |
| ACTIS Duofix Hip Prosthesis (K202472) | DePuy Orthopaedics, Inc. | 2020-10-21 |
| DePuy ATTUNE™ Total Knee System (K201347) | DePuy Orthopaedics, Inc. | 2020-06-18 |
| TRUMATCH Personalized Solutions (K193540) | DePuy Orthopaedics, Inc. | 2020-06-16 |