I.T.S. PRS Phoenix II
FDA 510(k) K260054 · I.T.S. GmbH
510(k) numberK260054
Submission
- Device name
- I.T.S. PRS Phoenix II
- Applicant
- I.T.S. GmbH
Laßnitzhöhe, AT - Received
- January 8, 2026
- Decision date
- April 24, 2026
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- HRS – Plate, Fixation, Bone
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3030
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code HRS
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261647 | Tempo Plating System; Ultra Compression Screw SystemHRS · Traditional | Pace Surgical | 09/03/2026SE |
| K261830 | FRAXION 3.5 Plate System (Various - See Catalog);FRAXION 4.5 Plate System (Various - See…HRS · Traditional | Ortler Global Tibbi Gerecler Anonim Sirketi | 08/28/2026SE |
| K262537 | Versalock Sterile Plating SystemHRS · Special | GM Dos Reis Industria e Comercio Ltda. | 08/19/2026SE |
| K260277 | Mikron Trauma Bone Plate& Screw SystemHRS · Traditional | Mikron Makina San. ve Tic. Ltd. Sti. | 08/13/2026SE |
| K261511 | Xpert AnkleHRS · Traditional | Newclip Technics | 07/28/2026SE |
| K261406 | Versalock Proximal Tibial Plating SystemHRS · Traditional | GM Dos Reis Industria e Comercio Ltda. | 07/21/2026SE |
| K262032 | TriMed Non-Spanning Wrist Fusion Plates (NSFL-STD);TriMed Non-Spanning Wrist Fusion…HRS · Special | TriMed, Inc. | 07/16/2026SE |
| K261191 | Alians Elbow SHRS · Traditional | Newclip Technics | 07/08/2026SE |
| K261054 | RibPlate SystemHRS · Traditional | Stryker Leibinger GmbH & Co KG | 07/01/2026SE |
| K261351 | SALGINA 2.5mm Distal Radius SystemHRS · Traditional | Bonebridge AG | 06/26/2026SE |
More from Bonebridge AG
| 510(k) | Device | Decision |
|---|---|---|
| K260958 | I.T.S. Clavicle Plates with Angular Stability; I.T.S. Volar Radius Plate with Angular…HRS · Traditional | 06/16/2026SE |
| K233134 | I.T.S. INS Proximal Femur NailHSB · Traditional | 02/12/2024SE |
| K210935 | I.T.S. Pelvic Reconstruction System (PRS RX & PRS Phoenix)HRS · Traditional | 08/31/2022SE |
| K142418 | I.T.S. Hand Locking Plates System - HLSHRS · Traditional | 09/26/2014SE |
| K132945 | Cfn-Cannulated Femur Nail, Ctn-Cannulated Tibia Nail, Chn-Cannulated Humeral NailHSB · Traditional | 03/07/2014SE |
| K131722 | I.T.S. Extremity Fixation SystemsHRS · Traditional | 08/07/2013SE |
| K130008 | Distal Ulna Locking Plate (Dul), Ulna Osteotomy Locking Plate (Uol), 3.0 Cancellous…HRS · Traditional | 06/25/2013SE |
Questions and answers
When was I.T.S. PRS Phoenix II cleared by the FDA?
I.T.S. PRS Phoenix II (K260054) received a 510(k) decision of Substantially Equivalent on April 24, 2026, 106 days after the submission was received.
What is the product code of K260054?
The FDA product code is HRS – Plate, Fixation, Bone, a Class II (moderate risk) device regulated under 21 CFR 888.3030.