Cleared Traditional

K854963 - S80 IMPLANTABLE CARDIAC PACING LEAD

K854963 is the FDA 510(k) clearance for S80 IMPLANTABLE CARDIAC PACING LEAD by Sorin Biomedica, Fiat, USA, Inc.. It is a Class 3 Cardiovascular device (product code DTB) cleared through the Traditional 510(k) pathway after a 195-day FDA review.

K854963 · Sorin Biomedica, Fiat, USA, Inc. · Cardiovascular device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1986
Decision
195d
Days
Class 3
Risk

K854963 is an FDA 510(k) clearance for the S80 IMPLANTABLE CARDIAC PACING LEAD. Classified as Permanent Pacemaker Electrode (product code DTB), Class III - Premarket Approval.

Submitted by Sorin Biomedica, Fiat, USA, Inc. (Italy, IT). The FDA issued a Cleared decision on June 24, 1986 after a review of 195 days - an extended review cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.3680 - 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 Sorin Biomedica, Fiat, USA, Inc. devices

Submission Details

510(k) Number K854963 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 11, 1985
Decision Date June 24, 1986
Days to Decision 195 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
70d slower than avg
Panel avg: 125d · This submission: 195d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code DTB Permanent Pacemaker Electrode
Device Class Class 3 - Premarket Approval
CFR Regulation 21 CFR 870.3680
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 - DTB Permanent Pacemaker Electrode

All 273
Devices cleared under the same product code (DTB) and FDA review panel - the closest regulatory comparables to K854963.
MODEL 438-01 CARDIFIX IMPLANTABLE PACING LEAD
K862052 · Intermedics, Inc. · Jul 1986
MODEL 435-02 CARDIFIX IMPLANTABLE PACING LEAD
K862276 · Intermedics, Inc. · Jul 1986
CORDIS HI-FLEX PERVENOUS BIPOLAR LEAD
K860846 · Cordis Corp. · Jun 1986
MODEL 486-02 ENDOCARDIAL PACING LEAD
K860547 · Intermedics, Inc. · Jun 1986
MODEL 492-02 ENDOCARDIAL PACING LEAD
K860548 · Intermedics, Inc. · Jun 1986
ENDOCARDIAL CARBON-TIP LEAD
K861481 · Pacesetter Systems · Jun 1986