Cleared Traditional

K040683 - BIODERM SCIENCES WOUND DRESSING

K040683 · Bioderm Sciences, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2004
Decision
80d
Days
-
Risk

K040683 is an FDA 510(k) clearance for the BIODERM SCIENCES WOUND DRESSING. Classified as Dressing, Wound, Drug (product code FRO).

Submitted by Bioderm Sciences, Inc. (Gaithersburg, US). The FDA issued a Cleared decision on June 4, 2004 after a review of 80 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 Bioderm Sciences, Inc. devices

FDA 510(k) Submission Details - K040683

510(k) Number K040683 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 16, 2004
Decision Date June 04, 2004
Days to Decision 80 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
35d faster than avg
Panel avg: 115d · This submission: 80d
Pathway characteristics
Predicate-based equivalence.

FRO Device Classification - Class 0,

Product Code FRO Dressing, Wound, Drug
Device Class -

Regulatory Peers - FRO Dressing, Wound, Drug

All 334
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