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: DXZ FDA class 2

Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene

Cardiovascular

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The Intracardiac Patch and Pledget made from polyethylene terephthalate (PETP), polytetrafluoroethylene (PTFE), or polypropylene is a cardiovascular implant used to repair septal defects, reinforce suture lines, or reconstruct cardiac structures during open-heart surgery. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) clearance before marketing. The product code is DXZ and the applicable regulation is 21 CFR 870.3470, under the Cardiovascular medical specialty. This device is an implant.

510(k) Clearances

50+ matches
K Number
Device Name
PeriBeam® Pericardial Membrane
Vascutek Gelseal Patch, Vascutek Gelsoft Patch, Vascutek Thin Wall Carotid Patch
ADAPT Tissue
PhotoFix Decellularized Bovine Pericardium
VascuCel
CorMatrix Tyke
PremiPatch PTFE Pledget
PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair Patch
VASCU-GUARD Peripheral Vascular Patch
CORMATRIX ECM FOR VASCULAR REPAIR
CARDIOCEL
SYNOVIS COLLAGEN MATRIX (TBD)
SMI CARDIOVASCULAR PATCH
SMI CARDIOVASCULAR PACH
PATCH, PLEDGET AND INTRACARDIAC
ALBOSURE POLYESTER VASCULAR PATCH
CRYOPATCH SG PULMONARY HUMAN CARDIAC PATCH
CARDIO-WRAP
CRYOPATCH SG PULMONARY HEMI-ARTERY; TRUNK; BRANCH
EDWARDS BOVINE PERICARDIAL PATCH, MODEL 4700
MATRACELL DECELLULARIZED PULMONARY ARTERY PATCH ALLOGRAFT
CORMATRIX PATCH FOR CARDIAC TISSUE REPAIR
IVENA VASCULAR PATCH
PERIPRO PATCH
REGENSIS PERICARDIAL PATCH
PFA PATCH
PTFE FELTS AND PLEDGETS
PERI-STRIPS STAPLE LINE REINFORCEMENT - SLEEVE AND STRIP CONFIGURATIONS - AND PERI-STRIPS DRY STAPLE LINE REINFORCEMENT
CORRESTORE PATCH SYSTEM
PERIPATCH SHEET, MODELS 1.5P8, 4P4, 4P6, 6P8, 10P16, 1.5P16
CORRESTORE PATCH SYSTEM
CHASE CARDIOVASCULAR PATCH KIT
CHARE CARIOVASCULAR PATCH
CHASE CARDIOVASCULAR PATCH KIT
CHASE CARDIOVASCULAR PATCH KIT
CORRESTORE PATCH, MODELS 1.5P2, 2P3, 3P4; CORRESTORE SIZER, MODEL CRPS
PRECLUDE PERICARDIAL MEMBRANE
CHASE CARDIOVASCULAR PATCH
CHASE CARDIOVASCULAR PATCH
SURGISIS PERIPHERAL VASCULAR PATCH
ETHIBOND EXCEL VALVE LOOP SUTURE
CHASE CARDIOVASCULAR PATCH
FLUORO-TEX CARDIOVASCULAR PATCH
SULZER CARBOMEDICS CARDIOFIX PERICARDIUM
UNI-GRAFT K DV PATCH
ACUSEAL CARDIOVASCULAR PATCH
CV PERI-GUARD AND VASCU-GUARD
SHELHIGH NO-REACT VASCUPATCH
SHELHIGH NO-REACT PERICARDIAL PATCHES
PATCH,PLEDGET AND INTRACARDIAC,PETP,PTFE,POLYPROPYLENE

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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