Cleared Traditional

EXTRACTOR III (K820292) - FDA 510(k) Clearance

K820292 · The Anspach Effort, Inc. · General & Plastic Surgery device
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Mar 1982
Decision
27d
Days
-
Risk

K820292 is an FDA 510(k) clearance for the EXTRACTOR III.

Submitted by The Anspach Effort, Inc. (Mchenry, US). The FDA issued a Cleared decision on March 2, 1982 after a review of 27 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel. 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 The Anspach Effort, Inc. devices

Submission Details

510(k) Number K820292 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 03, 1982
Decision Date March 02, 1982
Days to Decision 27 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
88d faster than avg
Panel avg: 115d · This submission: 27d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -