Cleared Traditional

K121001 - COPRESSION SYSTEMS (MODELS CMP-001 AND CMP-002)

K121001 is an FDA 510(k) clearance for COPRESSION SYSTEMS (MODELS CMP-001 AND ..., manufactured by Novitas Medical, LLC. The device is a Class 2 Cardiovascular device with product code JOW cleared through the Traditional 510(k) pathway after a 15-day FDA review.

K121001 · Novitas Medical, LLC · Cardiovascular device
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Apr 2012
Decision
15d
Days
Class 2
Risk

K121001 is an FDA 510(k) clearance for the COPRESSION SYSTEMS (MODELS CMP-001 AND CMP-002). Classified as Sleeve, Limb, Compressible (product code JOW), Class II - Special Controls.

Submitted by Novitas Medical, LLC (Brea, US). The FDA issued a Cleared decision on April 17, 2012 after a review of 15 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.5800 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

FDA 510(k) Submission Details - K121001

510(k) Number K121001 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 02, 2012
Decision Date April 17, 2012
Days to Decision 15 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Statement
Third-party Review Yes - reviewed by an FDA-accredited third party
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
110d faster than avg
Panel avg: 125d · This submission: 15d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

JOW Device Classification - Class 2, Special Controls

Product Code JOW Sleeve, Limb, Compressible
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.5800
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Cardiovascular devices follow this clearance model.

Regulatory Consultant

Intertek Testing Services
WILLIAM J SAMMONS

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - JOW Sleeve, Limb, Compressible

All 342
Devices cleared under the same product code (JOW) and FDA review panel - the closest regulatory comparables to K121001.
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K121001 · COPRESSION SYSTEMS (MODELS CMP-001 AND CMP-002)
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