Cleared Traditional

ROTAX-II BI-PLANE CIRCULAR ARM (K870205) - FDA 510(k) Clearance

K870205 · B C Medical , Ltd. · Radiology device
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Mar 1987
Decision
45d
Days
-
Risk

K870205 is an FDA 510(k) clearance for the ROTAX-II BI-PLANE CIRCULAR ARM.

Submitted by B C Medical , Ltd. (Canada, CA). The FDA issued a Cleared decision on March 6, 1987 after a review of 45 days - a notably fast clearance cycle.

This device falls under the Radiology 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 B C Medical , Ltd. devices

Submission Details

510(k) Number K870205 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 20, 1987
Decision Date March 06, 1987
Days to Decision 45 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
62d faster than avg
Panel avg: 107d · This submission: 45d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code -
Device Class -