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: LGF FDA class 1

Component, Cast

Orthopedic

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A cast component is an orthopedic device accessory used in the application and maintenance of plaster or synthetic casts for immobilizing fractures, dislocations, and other musculoskeletal injuries. The device is FDA Class 1, the lowest risk category, subject only to general controls without requiring premarket notification. It carries product code LGF and is regulated under 21 CFR 888.5940 within the Orthopedic specialty. This device is exempt from Good Manufacturing Practice (GMP) regulations.

510(k) Clearances

31 matches
K Number
Device Name
SILVERSEAL TUBULAR WOUND DRESSING WITH X-STATIC
CLINITEX STOCKINETTE
CLINITEX CAST PADDING
PROTEC COTTON PADDING BANDAGE
QUICK-CAST IMMOBILIZER
CARAPACE STERILE CAST PADDING
ARTIFLEX(TM)
COOL CAST(R)
CARAGLAS XTRA SYNTHETIC CASTING TAPE
SYNTHETIC CAST TAPE
COLORED CASTING TAPE CARAGLAS(TM GREEN
CUSHION TREAD WALKING HEEL PRODUCT NO. 4183-135
CHILD WALKING HEEL PRODUCT NO. 4183-132
PEDESTAL WALKING HEEL PRODUCT NO. 4183-133
COLORED CASTING TAPE (RED AND BLUE)
OEC DESIGN ORTHOPEDIC CAST HEEL
AMERICAN ORTHOPAEDIC CAST CUTTER, MODEL 0295-200
AMERICAN ORTHOPAEDIC VACUUM 0295-250
AMERICAN ORTHOPAEDIC CAST CUTTER, MODEL 0295-202
DELTA-LITE CASTING RESIN
DELTA-LITE CASTING RESIN
VENT-A-CAST
MASTERFOOT CAST HEEL
MASTERHINGE
CAST TOE COVER
WALKING HEEL
SHOW'RBAG
STERILE ORTHOPEDIC STOCKINETTE
COBBLER'S CHIP SPLINTS
CONPHAR CAST HEELS
INSERTER, PLUG, BONE, LIDGE

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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