Cleared Traditional

K033523 - COLLAGEN-ORC ANTIMICROBIAL MATRIX

K033523 · Johnson & Johnson Medical, Ltd. · General & Plastic Surgery device
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Oct 2004
Decision
349d
Days
-
Risk

K033523 is an FDA 510(k) clearance for the COLLAGEN-ORC ANTIMICROBIAL MATRIX. Classified as Dressing, Wound, Drug (product code FRO).

Submitted by Johnson & Johnson Medical, Ltd. (Somerville, US). The FDA issued a Cleared decision on October 21, 2004 after a review of 349 days - an unusually long review period, suggesting complex equivalence evaluation.

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: Standard predicate-based submission. Elevated predicate reliance profile. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Johnson & Johnson Medical, Ltd. devices

FDA 510(k) Submission Details - K033523

510(k) Number K033523 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 07, 2003
Decision Date October 21, 2004
Days to Decision 349 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
234d slower than avg
Panel avg: 115d · This submission: 349d
Pathway characteristics
Predicate-based equivalence.

FRO Device Classification - Class 0,

Product Code FRO Dressing, Wound, Drug
Device Class -

Regulatory Peers - FRO Dressing, Wound, Drug

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