Cleared Traditional

K883755 - MODIFIED SPECTRAX SX/SXT & PASYS/PASYS ...

K883755 is the FDA 510(k) clearance for MODIFIED SPECTRAX SX/SXT & PASYS/PASYS ... by Medtronic Vascular. It is a Class 3 Cardiovascular device (product code DXY) cleared through the Traditional 510(k) pathway after a 76-day FDA review.

K883755 · Medtronic Vascular · Cardiovascular device
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Nov 1988
Decision
76d
Days
Class 3
Risk

K883755 is an FDA 510(k) clearance for the MODIFIED SPECTRAX SX/SXT & PASYS/PASYS ST MODELS. Classified as Implantable Pacemaker Pulse-generator (product code DXY), Class III - Premarket Approval.

Submitted by Medtronic Vascular (Minneapolis, US). The FDA issued a Cleared decision on November 17, 1988 after a review of 76 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 Medtronic Vascular devices

Submission Details

510(k) Number K883755 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 02, 1988
Decision Date November 17, 1988
Days to Decision 76 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
49d faster than avg
Panel avg: 125d · This submission: 76d
Pathway characteristics
Predicate-based equivalence.

Device Classification

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 338
Devices cleared under the same product code (DXY) and FDA review panel - the closest regulatory comparables to K883755.
AFP MODEL 262T PULSE GENERATOR
K884733 · Pacesetter Systems · Feb 1989
OPTIMA MPT AND SPT PACEMAKERS
K884411 · Telectronics, Inc. · Jan 1989
UNILITH 3 MODELS 7580/7583/7680/7683
K883037 · Ela Medical, Inc. · Jan 1989
MINIX 8340, 8341, 8342 MINIX-ST 8330, 8331
K884215 · Medtronic Vascular · Nov 1988
OPUS 3 PULSE GENERATORS MODELS 4003,4004,4023,4024
K882391 · Ela Medical, Inc. · Nov 1988
CARDIAC PACE. OPUS 4000 MODELS 4043/4044/4063/4066
K882427 · Ela Medical, Inc. · Sep 1988