Cleared Traditional

K791225 - BJORK-SHILEY AORTIC GRAFT VALVE PROSTH

K791225 is an FDA 510(k) clearance for BJORK-SHILEY AORTIC GRAFT VALVE PROSTH, manufactured by Shiley, Inc.. The device is a Class 3 Cardiovascular device with product code DXY cleared through the Traditional 510(k) pathway after a 38-day FDA review.

K791225 · Shiley, Inc. · Cardiovascular device
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Aug 1979
Decision
38d
Days
Class 3
Risk

K791225 is an FDA 510(k) clearance for the BJORK-SHILEY AORTIC GRAFT VALVE PROSTH. Classified as Implantable Pacemaker Pulse-generator (product code DXY), Class III - Premarket Approval.

Submitted by Shiley, Inc. (Mchenry, US). The FDA issued a Cleared decision on August 10, 1979 after a review of 38 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3610 - 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: High-complexity regulatory submission. High regulatory complexity profile. 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 Shiley, Inc. devices

FDA 510(k) Submission Details - K791225

510(k) Number K791225 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 03, 1979
Decision Date August 10, 1979
Days to Decision 38 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
87d faster than avg
Panel avg: 125d · This submission: 38d
Pathway characteristics
Predicate-based equivalence.

DXY Device Classification - Class 3, Premarket Approval

Product Code DXY Implantable Pacemaker Pulse-generator
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 870.3610
What this classification means

Class III devices typically require Premarket Approval (PMA) with clinical evidence. Clearance through 510(k) for Class III devices is granted only when substantial equivalence to a valid predicate can be established.

Regulatory Peers - DXY Implantable Pacemaker Pulse-generator

All 353
Devices cleared under the same product code (DXY) and FDA review panel - the closest regulatory comparables to K791225.
IMPLANTABLE PULSE GENERATOR PACEMAKER
K791417 · Intermedics, Inc. · Sep 1979
PULSE GENERATOR, R WAVE DEMAND
K790141 · Pacesetter Systems · Aug 1979
MDL-201A & T DL-201A PULSE GENERATOR
K790428 · Pacesetter Systems · Aug 1979
UNILITH PULSE GENERATOR
K791219 · Ela Medical, Inc. · Jul 1979
PULSE GENERATOR, MODEL 171
K782161 · Telectronics, Inc. · Jul 1979
BATTERY CHARGER, 171 PACEMAKER
K782162 · Telectronics, Inc. · Jul 1979