Cleared Traditional

K872858 - WILLIAMS VERTEBRAL SPREADER

K872858 is an FDA 510(k) clearance for WILLIAMS VERTEBRAL SPREADER, manufactured by Ace Medical Co.. The device is a Class 1 Orthopedic device with product code HXP cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K872858 · Ace Medical Co. · Orthopedic device
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Oct 1987
Decision
86d
Days
Class 1
Risk

K872858 is an FDA 510(k) clearance for the WILLIAMS VERTEBRAL SPREADER. Classified as Instrument, Bending Or Contouring (product code HXP), Class I - General Controls.

Submitted by Ace Medical Co. (Martinez, US). The FDA issued a Cleared decision on October 15, 1987 after a review of 86 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.4540 - 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 Ace Medical Co. devices

FDA 510(k) Submission Details - K872858

510(k) Number K872858 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 21, 1987
Decision Date October 15, 1987
Days to Decision 86 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
36d faster than avg
Panel avg: 122d · This submission: 86d
Pathway characteristics
Predicate-based equivalence.

HXP Device Classification - Class 1, General Controls

Product Code HXP Instrument, Bending Or Contouring
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 888.4540
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.