SPECTRUM GV Bone Cement
FDA 510(k) K250760 · Osteoremedies, LLC
510(k) numberK250760
Submission
- Device name
- SPECTRUM GV Bone Cement
- Applicant
- Osteoremedies, LLC
Memphis, TN, US - Received
- March 13, 2025
- Decision date
- April 2, 2025
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- LOD – Bone Cement
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3027
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code LOD
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K254107 | Refobacin Bone Cement R (110034355)LOD · Traditional | Biomet France | 04/15/2026SE |
| K241674 | Osteopal® VLOD · Traditional | Heraeus Medical GmbH | 12/05/2024SE |
| K231556 | SPECTRUM® GV Bone CementLOD · Traditional | Osteoremedies, LLC | 12/20/2023SE |
| K211163 | Bone Cement Genta, Bone Cement HV, Bone Cement LVLOD · Traditional | Tecres S.P.A. | 01/09/2023SE |
| K212729 | Bone Cement-Normal ViscosityLOD · Traditional | Biomecanica Industria E Comerciode Produtos… | 05/31/2022SE |
| K211869 | OGM 1 Polymethylmethacrylate (PMMA) bone cement, OGM 1A Polymethylmethacrylate (PMMA)…LOD · Traditional | Ormed Grup Medikal Turizm Saglik Hizmetleri… | 05/19/2022SE |
| K213812 | PALACOS MV proLOD · Traditional | Heraeus Medical GmbH | 02/02/2022SE |
| K210607 | PALACOS R pro, PALACOS R+G pro, PALACOS MV+G proLOD · Traditional | Heraeus Medical GmbH | 07/09/2021SE |
| K202458 | BonOs Inject, Pedicle screw kits, Cement pusherLOD · Traditional | Osartis GmbH | 05/18/2021SE |
| K210125 | BonOs HV Genta, BonOs MV Genta, BonOs LV GentaLOD · Traditional | Osartis GmbH | 03/19/2021SE |
More from Osartis GmbH
| 510(k) | Device | Decision |
|---|---|---|
| K262290 | REMEDY POLY+PLUS SNAP FIT Acetabular CupKWL · Special | 07/24/2026SE |
| K253675 | OsteoRemedies Hip Spacer SystemKWL · Special | 12/23/2025SE |
| K242377 | REMEDY Stemmed Knee Spacer System with All-Poly Tibial ComponentJWH · Traditional | 10/02/2024SE |
| K231556 | SPECTRUM® GV Bone CementLOD · Traditional | 12/20/2023SE |
| K223650 | REMEDY Stemmed Knee SpacerJWH · Special | 01/05/2023SE |
| K192995 | OsteoRemedies Hip Spacer SystemKWL · Special | 01/10/2020SE |
| K191981 | REMEDY Acetabular CupKWL · Special | 08/23/2019SE |
| K183017 | Remedy Femoral Component 84mm, Remedy Stemmed Knee SpacerJWH · Traditional | 07/25/2019SE |
| K172906 | REMEDY PLUS Hip Spacer, UNITE PLUS Bone CementKWL · Traditional | 08/29/2018SE |
| K173967 | Remedy Acetabular CupKWL · Traditional | 02/22/2018SE |
Questions and answers
When was SPECTRUM GV Bone Cement cleared by the FDA?
SPECTRUM GV Bone Cement (K250760) received a 510(k) decision of Substantially Equivalent on April 2, 2025, 20 days after the submission was received.
What is the product code of K250760?
The FDA product code is LOD – Bone Cement, a Class II (moderate risk) device regulated under 21 CFR 888.3027.