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: MQV FDA class 2

Filler, Bone Void, Calcium Compound

Orthopedic

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The Calcium Compound Bone Void Filler is an orthopedic implant made from calcium-based materials (such as calcium sulfate, calcium phosphate, or hydroxyapatite) used to fill bony defects and voids, supporting bone healing and regeneration. Classified as FDA Class 2 under 21 CFR 888.3045 in the Orthopedic specialty, it requires 510(k) premarket notification. The product code is MQV, and it carries an implant flag.

510(k) Clearances

50+ matches
K Number
Device Name
OsteoFlo HydroFiber
Grafton™ DBM; Grafton Plus™ DBM Paste; Magnifuse™ Bone Graft
OsteoFlo HydroFiber
MagnetOs MIS
Synthecure Synthetic Calcium Sulfate
NanoBone® SBX Putty ; NanoBone® QD
Porous Biologic Scaffold
BonVie+
Moldable Bone Void Filler and Moldable Bone Void Filler + CCC
Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules
OsteoFlo HydroFiber
GlassBone Granules
BioSphere Putty; BioSphere MIS Putty
EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone )
Porous Biologic Scaffold
MONTAGE Settable, Resorbable Bone Putty MONTAGE-QS Settable, Resorbable Bone Putty MONTAGE Flowable Settable, Resorbable Bone Paste MONTAGE-XT Settable, Resorbable Hemostatic Bone Putty
Montage-XT Settable Bone Putty
Device 300397 Putty
Citrepore™
Mg OSTEOREVIVE™, Mg OSTEOCRETE™
Cove Putty, OsteoCove Putty
NovaBone Putty - Synthetic Bioactive Bone Graft
Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip, Vitoss® BiModal Bioactive Bone Graft Substitute, Vitoss BBTrauma® Bioactive Bone Graft Substitute,Vitoss® BA2X Bioactive Bone Graft Substitute, Vitoss® Bioactive Bone Graft Substitute Pack,Vitoss® Bioactive Bone Graft Substitute, Vitoss® Foam Bone Graft Substitute, Vitoss® Bone Graft Substitute Filled Canister, Vitoss® Bone Graft Substitute, Vitoss® Bone Graft Substitute - Synthetic Cancellous Chips
Montage-XT Settable, Resorbable Bone Putty
Actifuse ABX; Actifuse MIS; Actifuse Shape; ALTAPORE; ALTAPORE SHAPE; ALTAPORE MIS
Montage Settable Bone Putty
MagnetOs Easypack Putty
Xerosyn
Morpheus® Moldable; Agilon® Moldable
MagnetOs Putty
NuVasive AttraX Scaffold
Mineral Collagen Composite Bioactive Moldable Bone Graft Matrix
Synthetic Bone Putty
Cerament Bone Void Filler
NovaBone Putty - Bioactive Synthetic Bone Graft (NB6600, NB6610, NB6615)
ReBOSSIS
Mg OSTEOINJECT™; Mg OSTEOREVIVE™; Mg OSTEOCRETE™
MagnetOs Granules
Tactoset® Injectable Bone Substitute
MagnetOs Putty
MagnetOs Easypack Putty
SIGNAFUSE Bioactive Strip (SBS); SIGNAFUSE Putty
MagnetOs Flex Matrix
OsteoFlo® HydroPutty™
Cove Strip, OsteoCove Strip
Catalyst Bone Void Filler
Cove Putty, OsteoCove Putty
Montage Flowable Settable, Resorbable Bone Paste
Montage-QS Settable, Resorbable Bone Putty
Cove Strip

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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