Cleared Traditional

K162500 - Ostial Sprit Cannulae

K162500 is an FDA 510(k) clearance for Ostial Sprit Cannulae, manufactured by Spyder Medical. The device is a Class 2 Cardiovascular device with product code DWF cleared through the Traditional 510(k) pathway after a 127-day FDA review.

K162500 · Spyder Medical · Cardiovascular device
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Jan 2017
Decision
127d
Days
Class 2
Risk

K162500 is an FDA 510(k) clearance for the Ostial Sprit Cannulae. Classified as Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass (product code DWF), Class II - Special Controls.

Submitted by Spyder Medical (Rancho Santa Margarita, US). The FDA issued a Cleared decision on January 12, 2017 after a review of 127 days - within the typical 510(k) review window.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4210 - 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 Spyder Medical devices

FDA 510(k) Submission Details - K162500

510(k) Number K162500 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 07, 2016
Decision Date January 12, 2017
Days to Decision 127 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
2d slower than avg
Panel avg: 125d · This submission: 127d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DWF Device Classification - Class 2, Special Controls

Product Code DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4210
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 - DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

All 301
Devices cleared under the same product code (DWF) and FDA review panel - the closest regulatory comparables to K162500.
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