Cleared Traditional

K890350 - VS-1 SILICONE IMPLANT LEADS (NEW SERIAL...

K890350 is an FDA 510(k) clearance for VS-1 SILICONE IMPLANT LEADS (NEW SERIAL..., manufactured by Telectronics, Inc.. The device is a Class 3 Cardiovascular device with product code DTB cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K890350 · Telectronics, Inc. · Cardiovascular device
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Feb 1989
Decision
86d
Days
Class 3
Risk

K890350 is an FDA 510(k) clearance for the VS-1 SILICONE IMPLANT LEADS (NEW SERIAL # TUBE). Classified as Permanent Pacemaker Electrode (product code DTB), Class III - Premarket Approval.

Submitted by Telectronics, Inc. (Englewood, US). The FDA issued a Cleared decision on February 2, 1989 after a review of 86 days - a notably fast clearance 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 Telectronics, Inc. devices

FDA 510(k) Submission Details - K890350

510(k) Number K890350 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 08, 1988
Decision Date February 02, 1989
Days to Decision 86 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
39d faster than avg
Panel avg: 125d · This submission: 86d
Pathway characteristics
Predicate-based equivalence.

DTB Device Classification - Class 3, Premarket Approval

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 387
Devices cleared under the same product code (DTB) and FDA review panel - the closest regulatory comparables to K890350.
MODELS 432-03 & 433-03 IMPLANTABLE PACING LEADS
K890411 · Intermedics, Inc. · Mar 1989
MODELS 430-07 & 431-07 IMPLANTABLE PACING LEADS
K890412 · Intermedics, Inc. · Mar 1989
SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS
K890547 · Pacesetter Systems · Mar 1989
MODEL 6208,6209,6210,6211,6212,6214 (PLI'S)
K890045 · Medtronic Vascular · Jan 1989
MEDTRONIC MODEL 4058 PACING LEAD
K883743 · Medtronic Vascular · Jan 1989
IMPLANTABLE ELECTRODE LEADS 033-400,402 AND 436
K884278 · Telectronics, Inc. · Dec 1988