Cleared Traditional

K932024 - CCG CERCLAGE SYSTEM

K932024 is an FDA 510(k) clearance for CCG CERCLAGE SYSTEM, manufactured by Encore Orthopedics, Inc.. The device is a Class 2 Orthopedic device with product code JDQ cleared through the Traditional 510(k) pathway after a 659-day FDA review.

K932024 · Encore Orthopedics, Inc. · Orthopedic device
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Feb 1995
Decision
659d
Days
Class 2
Risk

K932024 is an FDA 510(k) clearance for the CCG CERCLAGE SYSTEM. Classified as Cerclage, Fixation (product code JDQ), Class II - Special Controls.

Submitted by Encore Orthopedics, Inc. (Austin, US). The FDA issued a Cleared decision on February 14, 1995 after a review of 659 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3010 - the FDA orthopedic device regulatory 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. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Orthopedic submissions.

View all Encore Orthopedics, Inc. devices

FDA 510(k) Submission Details - K932024

510(k) Number K932024 FDA.gov
FDA Decision Cleared Substantially Equivalent - NSE Converted (SN)
Date Received April 26, 1993
Decision Date February 14, 1995
Days to Decision 659 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
537d slower than avg
Panel avg: 122d · This submission: 659d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JDQ Device Classification - Class 2, Special Controls

Product Code JDQ Cerclage, Fixation
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3010
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 Orthopedic devices follow this clearance model.

Regulatory Peers - JDQ Cerclage, Fixation

All 90
Devices cleared under the same product code (JDQ) and FDA review panel - the closest regulatory comparables to K932024.
DALL MILES SYSTEM HOMOGENEOUS VITALLIUM CABLE
K945294 · Howmedica Corp. · Mar 1995
CABLE-EASE PLATE AND CABLE SYSTEM - TROCHANTERIC HOOK
K950027 · Intermedics Orthopedics · Mar 1995
CABLE-EASE PLATE AND CABLE SYSTEM
K944529 · Intermedics Orthopedics · Feb 1995
PIONEER LABORATORIES BONE PLATE WITH CERCLAGE CABLES
K940729 · Pioneer Surgical Technology · Dec 1994
DALL MILES SYSTEM GROOVED BUTTON
K934059 · Howmedica Corp. · Aug 1994
SONGER CABLE SYSTEM
K941213 · Pioneer Surgical Technology · Apr 1994