Cleared Traditional

K974706 - AESCULAP ABC CERVICAL PLATING SYSTEM

K974706 is the FDA 510(k) clearance for AESCULAP ABC CERVICAL PLATING SYSTEM by Aesculap, Inc.. It is a Class 2 Orthopedic device (product code KWQ) cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K974706 · Aesculap, Inc. · Orthopedic device
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Mar 1998
Decision
87d
Days
Class 2
Risk

K974706 is an FDA 510(k) clearance for the AESCULAP ABC CERVICAL PLATING SYSTEM. Classified as Appliance, Fixation, Spinal Intervertebral Body (product code KWQ), Class II - Special Controls.

Submitted by Aesculap, Inc. (South San Francisco, US). The FDA issued a Cleared decision on March 13, 1998 after a review of 87 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3060 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Aesculap, Inc. devices

Submission Details

510(k) Number K974706 FDA.gov
FDA Decision Cleared Substantially Equivalent - NSE Converted (SN)
Date Received December 16, 1997
Decision Date March 13, 1998
Days to Decision 87 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
35d faster than avg
Panel avg: 122d · This submission: 87d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KWQ Appliance, Fixation, Spinal Intervertebral Body
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3060
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 - KWQ Appliance, Fixation, Spinal Intervertebral Body

All 447
Devices cleared under the same product code (KWQ) and FDA review panel - the closest regulatory comparables to K974706.
BLACKSTONE MEDICAL INC. ANTERIOR CERVICAL PLATE SYSTEM
K974885 · Blackstone Medical, Inc. · Jun 1998
UNIVERSITY PLATE ANTERIOR SYSTEM
K980228 · Acromed Corp. · Apr 1998
ORION ANTERIOR CERVICAL PLATE SYSTEM
K973854 · Sofamor Danek USA,Inc. · Mar 1998
KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS
K974757 · Acromed Corp. · Mar 1998
SYNTHES SPINE ANTERIOR THORACOLUMBAR ROD CLAMP (ATRC) SYSTEM
K974525 · Synthes Spine · Mar 1998
MICHELSON ANTERIOR CERVICAL PLATE SYSTEM
K974435 · Wrightmedicaltechnologyinc · Feb 1998