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: HCH FDA class 2

Clip, Aneurysm

Neurology

View full classification →

The Aneurysm Clip is a permanently implanted neurosurgical device placed across the neck of an intracranial aneurysm during open surgery to exclude it from the cerebral circulation and prevent rupture or rebleeding. It is classified as a Class 2 device (moderate risk), requiring 510(k) premarket notification, and is designated as an implant. The product code is HCH under regulation 21 CFR 882.5200 in the Neurology specialty. The implant flag is active for this device.

510(k) Clearances

36 matches
K Number
Device Name
Sugita AVM Microclips
D-Clip; D-Clip Applier
YASARGIL ANEURYSM CLIPS AND CLIP APPLIERS
CODMAN ANEURYSM CLIPS, CODMAN AVM MICRO CLIP SYSTEM, CODMAN SLIM-LINE GRAFT, REINFORCING, MINI ANEURYSM CLIP
GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS
L-ANEURYSM-CLIP SYSTEM & L-ANEURYSM CLIP APPLIERS, YASARGIL ANEURYSM CLIPS & YASARGIL ANEURYSM CLIP APPLIERS
KIRWAN L-ANEURYSM CLIPS AND APPLIER, KIRWAN YASARGIL-TYPE ANEURYSM CLIPS AND APPLIERS
AESCULAP T-BAR ANEURYSM CLIPS (TITANIUM & PHYNOX)
AESCULAP YASARGIL ANEURYSM CLIP PHYNOX BOOSTER CLIP
TEMPORARY TITANIUM ANEURYSM CLIP
AESULAP KOPITNIK AVM MICROCLIPS AND APPLIER
ANEURYSM CLIPS
MEDICON TITANIUM YASARGIL ANEURYSM CLIPS
REBSTOCK YASARGIL ANEURYSM CLIP
YASARGIL PERMANENT ANEURYSM CLIPS
MODIFICATION TO YASARGIL ANEURYSM CLIPS
PSI TITANIUM ANEURYSM CLIP
SUGITA TITANIUM ANEURYSM CLIP
YASARGIL TITANIUM ANEURYSM CLIPS
TAKA ANEURYSM CLIP
YASARGIL TITANIUM ANEURYSM CLIPS (FTXXXT)
SUGITA AVM MICROCLIP
SPETZLER TI 100 ANEURYSM CLIP
SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM
SUNDT SLIM-LINE GRAFT CLIPS
YASARGIL ANEURYSM CLIPS
YASARGIL ANEURYSM CLIPS, MODIFICATION
PERNECZKY ANEURYSM CLIP
SUNDT-KEES REINFORCING ANEURYSM CLIP
YASARGIL FENESTRATED ANEURYSM CLIP &
YASARGIL STANDARD ANEURYSM CLIP &
HEIFETZ INTRACRANIAL ANEURYSM CLIPS
SCOVILLE-LEWIS ANEURYSM CLIPS
HEIFETZ ANEURYSM CLIP, LMM BLADE
YASARGIL ANEURYSM CLIPS
OCCLUSION CLIPS

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.

Popular Product Codes

Commonly searched