Cleared Traditional

K790877 - BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO (FDA 510(k) Clearance)

Class I Orthopedic device.

K790877 · Stackhouse Assoc. · Orthopedic device
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May 1979
Decision
16d
Days
Class 1
Risk

K790877 is an FDA 510(k) clearance for the BIOVAC: LFA LASER FUME (SMOKE) EVACUATIO. Classified as Evacuator, Vapor, Cement Monomer (product code JDY), Class I - General Controls.

Submitted by Stackhouse Assoc. (Walker, US). The FDA issued a Cleared decision on May 23, 1979 after a review of 16 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.4220 - 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 Stackhouse Assoc. devices

Submission Details

510(k) Number K790877 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 07, 1979
Decision Date May 23, 1979
Days to Decision 16 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
106d faster than avg
Panel avg: 122d · This submission: 16d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JDY Evacuator, Vapor, Cement Monomer
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 888.4220
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.