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: HTN FDA class 2

Washer, Bolt Nut

Orthopedic

View full classification →

A bolt nut washer is a small metal orthopedic hardware component used in conjunction with bone screws and bolts to secure internal fixation implants during bone fracture repair or spinal stabilization. It is classified as an FDA Class 2 device under 21 CFR 888.3030, indicating moderate risk and requiring 510(k) premarket clearance. Product code HTN falls under the Orthopedic medical specialty. This device is an implant.

510(k) Clearances

50+ matches
K Number
Device Name
RipCord
Acu-Sinch Knotless Mini
Bolo Button System
TACTIX Vector Syndesmosis System
EXPERT - Flexible Joint Fixation System
TACTIX Vector Syndesmosis System
TENSOR® Suture Button System
OIC FLEX-FIX™ System
CC-Clip® Implant System
Arthrex FiberTape and TigerTape Cerclage Sutures
Arthrex FiberTape and TigerTape Cerclage Sutures
Arthrex Knotless AC Repair Devices
TriMed Ripcord Device
Hercules Syndesmosis Implant System
Acumed Ankle Syndesmosis Repair System
Arthrex Knotless Mini TightRopes
Medline UNITE REFLEX Dynamic Discs
EXPERT - Joint Fixation System
Arthrex Syndesmosis TightRope XP Buttress Plate Implant System
Akros Scruture Anchor LisFranc Repair Kit
LARS AC Band Device
MicroLink All-Suture Button Fixation System (Radiolucent)
MicroLink All-Suture Button Fixation System (Radiopaque)
CyclaPlex Correction System
Double ENDOBUTTON Fixation Device
Infinity-Lock Button System
PUMA System
Akros FibuLink™ Syndesmosis Repair Kit
SyndesMetrics Syndesmosis Repair System
GRAVITY™ Syndesmosis LP
INVISIKNOT Ankle Syndesmosis Repair Kit
KISSloc Suture System
Akros Fibulink Syndesmosis Repair Kit
M-Fix Acromioclavicular Device
Tensyn Plug
Tensyn Plug
FASTFORWARD
TENSYN BAND, TENSYN FRACTURE PLATES
JUGGERLOC BONE TO BONE IMPLANTS/ BONE INSTRUMENTS/ BONE IMPLANT AND INSTRUMENT KITS
ARTHROSURFACE KISSLOC KNOTLESS SUTURE SYSTEM
CMC MINI TIGHTROPE
TENSYN BAND
MINI TIGHTROPE
ORTHOHELIX SYNDESMOSIS FIXATION DEVICES
TENSYN BAND
BIOPRO - INFINITY PLATE ANCHOR SYSTEM
FRAG-LOC SYSTEM
ARTHREX FRACTURE SYSTEM
ACU-SINCH REPAIR SYSTEM AND ACUMED SUTURE ANCHOR
CMC CABLE FIX

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