Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: LOD FDA class 2

Bone Cement

Orthopedic

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Bone Cement is a polymeric material, typically based on polymethylmethacrylate (PMMA), used in orthopedic and spinal surgery to fix prosthetic implants to bone or to fill bone defects, providing mechanical fixation and load transfer between the implant and the surrounding osseous tissue. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) premarket clearance. The product code is LOD, regulated under 21 CFR 888.3027, within the Orthopedic medical specialty. This device is an implant.

510(k) Clearances

50+ matches
K Number
Device Name
SPECTRUM GV Bone Cement
OSTEOPAL® V
SPECTRUM® GV Bone Cement
Bone Cement Genta, Bone Cement HV, Bone Cement LV
Bone Cement-Normal Viscosity
OGM 1 Polymethylmethacrylate (PMMA) bone cement, OGM 1A Polymethylmethacrylate (PMMA) bone cement
PALACOS MV pro
PALACOS R pro, PALACOS R+G pro, PALACOS MV+G pro
BonOs Inject, Pedicle screw kits, Cement pusher
BonOs HV, BonOs MV, BonOs LV
BonOs HV Genta, BonOs MV Genta, BonOs LV Genta
PALACOS R, PALACOS R pro, PALACOS R+G, PALACOS R+G pro, PALACOS MV+G
G3 40 Radiopaque Bone Cement
G1 40 Radiopaque Bone Cement
Hi-Fatigue Bone Cement
Hi-Fatigue G Bone Cement
PALACOS fast R+G
G3A 40 Bone Cement
PALACOS MV
OrthoSteady G Bone Cement
Biomet Bone Cement R
TRAUMACEM™ V+ Injectable Bone Cement
Refobacin Bone Cement R
OSTEOPAL plus
V-STEADY, V-FAST
PALACOS R pro
NP Cement HV;NP Cement LV; NP Cement HV System; NP Cement LV System
NP Cement HV Genta;NP Cement LV Genta;NP Cement HV System Genta;NP Cement LV System Genta
PALACOS R+G PRO
BONOS R 1X20, BONOS R 2X20, BONOS R 1X40, BONOS R 2X40, BONOS R 1X60
BONOS R GENTA 1X20 MODEL 01-0228; BONOS R GENTA 2X20 MODEL 01-0229; BONOS R GENTA 1X40 MODEL 01-0217; BONOS R GENTA 2X40
CEMEX GENTA, GENTA SYSTEM AND GENTA SYSTEM FAST
COBALT MV WITH GENTAMICIN (AKA COBALT G-MV) BONE CEMENT
COBALT MV BONE CEMENT
SMARTSET MV BONE CEMENT
COBALT V RADIOPAQUE VERTEBROPLASTY BONE CEMENT
SIMPLEX P BONE CEMENT
SIMPLEX P SPEEDSET BONE CEMENT
SMARTMIX CEMVAC PRE-FILLED WITH SMARTSET HV BONE CEMENT
DEPUY CMW 1, 2 AND 3 BONE CEMENTS
OSTEOPAL V
COBALT BONE CEMENT
COBALT G HV BONE CEMENT
PALACOS LV+G
PALAMED G
CEMEX SYSTEM GENTA FAST BONE CEMENT
MODIFICATION TO DEPUY 1 GENTAMICIN BONE CEMENT AND SMARTSET GMV ENDURANCE GENTAMICIN BONE CEMENT
REFOBACIN -PALACOS G
SIMPLEX X
CEMEX GENTA BONE CEMENT; CEMEX GENTA SYSTEM BONE CEMENT

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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