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: HAE FDA class 2

Rongeur, Manual

Neurology

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The Manual Rongeur is a hand-held neurosurgical instrument with a strong, hinged jaw used to bite away and remove small pieces of bone or other hard tissue during cranial and spinal surgical procedures. It is classified as a Class 2 device (moderate risk), requiring 510(k) premarket notification. The product code is HAE under regulation 21 CFR 882.4840 in the Neurology specialty. It is eligible for third-party 510(k) review.

510(k) Clearances

36 matches
K Number
Device Name
Geister K-Rex rongeurs
SQ.line KERRISON
Rebellion, Phantom Multi-Bite Kerrison Rongeur
Rebellion; Phantom Multi-Bite Kerrison Rongeur
KLS Martin Neuro Rongeurs
Rebellion, Phantom Multi-Bite Kerrison Rongeur
Ace Medical Surgical Instruments
Wiggins Medical Surgical Instruments
Steribite
Symmetry Sharp Kerrison Rongeur
Fehling-Punches
Kerrison Rongeurs
Laminectomy Rongeurs, Kerrison Rongeurs, IVD Rongeurs
Integra (R) Jarit (R) Kerrison Rongeurs, Integra (R) Ruggles (TM)-Redmons (TM) Kerrison Rongeurs, Integra (R) Miltex (R) Kerrison Rongeurs, Integra (R) Meisterhand (R) Kerrison Rongeurs
OSTEOMED NEURO RONGEUR
SYMMETRY KERRISON DISPOSABLE TIP RONGEURS
IO-TOME DEVICE
NEURO CHECK DEVICE WITH IO-FLEX WIRE
MODIFICATION TO: MICROBLADE SHAVER AND ACCESSORIES
JARIT, RUGGLES, R&B REDMOND/ REDMOND, MILTEX, MEISTERHAND - KERRISON RONGEURS
INSTRUMED RONGEUR
BAXANO ULTRA LOW PROFILE RONGEUR
MICROBLADE SHAVER AND ACCESSORIES
ULTRA LOW PROFILE RONGEUR
DAN KERRISON RONGEURS, MODELS K1 + BILLY 1
BRAY RONGEUR
KERRISON RONGEURS
ULTRA-LINE RONGEUR
AUTO SUTURE KERRISON SPINAL RONGEUR
NEDBOND EJECTOR KERRISON RONGEUR
INTERVERTEBRAL DISC RONGEUR
SPECIAL RONGEUR
INSTRUMENTS FOR NEUROLOGICAL SURGERY
LAMINECTOMY RONGEUR
NEUROLOGICAL RONGEURS - VARIOUS TYPES
RONGEUR (NEUROSURGICAL INSTRUMENTS)

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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