Cleared Traditional

K852435 - CCS IMPLANTABLE MAESTRO SERIES 100 CARD...

K852435 is the FDA 510(k) clearance for CCS IMPLANTABLE MAESTRO SERIES 100 CARD... by Cardiac Control Systems, Inc.. It is a Class 3 Cardiovascular device (product code DXY) cleared through the Traditional 510(k) pathway after a 57-day FDA review.

K852435 · Cardiac Control Systems, Inc. · Cardiovascular device
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Aug 1985
Decision
57d
Days
Class 3
Risk

K852435 is an FDA 510(k) clearance for the CCS IMPLANTABLE MAESTRO SERIES 100 CARDIAC PACEMA. Classified as Implantable Pacemaker Pulse-generator (product code DXY), Class III - Premarket Approval.

Submitted by Cardiac Control Systems, Inc. (Palm Coast, US). The FDA issued a Cleared decision on August 6, 1985 after a review of 57 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 Cardiac Control Systems, Inc. devices

Submission Details

510(k) Number K852435 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 10, 1985
Decision Date August 06, 1985
Days to Decision 57 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
68d faster than avg
Panel avg: 125d · This submission: 57d
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 340
Devices cleared under the same product code (DXY) and FDA review panel - the closest regulatory comparables to K852435.
NEOS - M ABP
K853058 · Biotronik Sales, Inc. · Sep 1985
TRIOS - M
K853057 · Biotronik Sales, Inc. · Sep 1985
IMPLANT PROGRAM CARDIAC PULSE GEN W/MOD SET SCREW
K853206 · Telectronics, Inc. · Sep 1985
ELA MEDICAL CARDIAC PACEMAKERS MULTIL 2 #1251&2251
K853017 · Ela Medical, Inc. · Jul 1985
#335-01 SILIC RUB ISOLA SLEEVE FOR INT #281-03 SIZ
K853034 · Intermedics, Inc. · Jul 1985
SUPRIMA II MODEL 254-26
K852431 · Intermedics, Inc. · Jul 1985