Cleared Traditional

K150709 - ProTrack RF Anchor Wire

K150709 is an FDA 510(k) clearance for ProTrack RF Anchor Wire, manufactured by Baylis Medical Company, Inc.. The device is a Class 2 Cardiovascular device with product code DXF cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K150709 · Baylis Medical Company, Inc. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2015
Decision
90d
Days
Class 2
Risk

K150709 is an FDA 510(k) clearance for the ProTrack RF Anchor Wire. Classified as Catheter, Septostomy (product code DXF), Class II - Special Controls.

Submitted by Baylis Medical Company, Inc. (Mississauga, CA). The FDA issued a Cleared decision on June 17, 2015 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.5175 - the FDA cardiovascular device oversight framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

View all Baylis Medical Company, Inc. devices

FDA 510(k) Submission Details - K150709

510(k) Number K150709 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 19, 2015
Decision Date June 17, 2015
Days to Decision 90 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
35d faster than avg
Panel avg: 125d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DXF Device Classification - Class 2, Special Controls

Product Code DXF Catheter, Septostomy
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.5175
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Peers - DXF Catheter, Septostomy

All 20
Devices cleared under the same product code (DXF) and FDA review panel - the closest regulatory comparables to K150709.
Fogarty Dilation Atrioseptostomy Catheter, Miller Balloon Atrioseptostomy Catheter
K221528 · Edwards Lifesciences, LLC · Aug 2022
Z-6 Atrioseptostomy Catheter
K211910 · NuMED, Inc. · Jul 2021
Park Blade Septostomy Catheter
K182399 · Cook Incorporated · Apr 2019
NRG TRANSSEPTAL NEEDLE
K073326 · Baylis Medical Co., Inc. · May 2008
TORONTO RF SEPTOSTOMY CATHETER, MODEL TSC-50-75
K031949 · Baylis Medical Co., Inc. · Dec 2003
PTA, PTV, ATRIOSEPTOSTOMY, ANGIOGRAPHIC, SIZING CATHETERS
K011557 · NuMED, Inc. · Jul 2001