Cleared Traditional

K092233 - SURGIMESH XD

K092233 is an FDA 510(k) clearance for SURGIMESH XD, manufactured by Aspide Medical. The device is a Class 2 General & Plastic Surgery device with product code FTL cleared through the Traditional 510(k) pathway after a 337-day FDA review.

K092233 · Aspide Medical · General & Plastic Surgery device
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Jun 2010
Decision
337d
Days
Class 2
Risk

K092233 is an FDA 510(k) clearance for the SURGIMESH XD. Classified as Mesh, Surgical, Polymeric (product code FTL), Class II - Special Controls.

Submitted by Aspide Medical (Washington, US). The FDA issued a Cleared decision on June 25, 2010 after a review of 337 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.3300 - the FDA general and plastic surgery device framework. 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 Aspide Medical devices

FDA 510(k) Submission Details - K092233

510(k) Number K092233 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 23, 2009
Decision Date June 25, 2010
Days to Decision 337 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
222d slower than avg
Panel avg: 115d · This submission: 337d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FTL Device Classification - Class 2, Special Controls

Product Code FTL Mesh, Surgical, Polymeric
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.3300
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - FTL Mesh, Surgical, Polymeric

All 210
Devices cleared under the same product code (FTL) and FDA review panel - the closest regulatory comparables to K092233.
RENASYS F/-AB ABDOMINAL WOUND DRESSING KIT
K100787 · Smith & Nephew, Inc. · Sep 2010
ASCEND BLUE AC MESH
K101462 · Caldera Medical, Inc. · Aug 2010
VENTRALIGHT ST MESH
K101851 · Davol Inc., Sub. C. R. Bard, Inc. · Jul 2010
PARIE TENE PROGRIP MESH
K101197 · Sofradim Production · May 2010
TORNIER SURGICAL MESH
K093799 · Tornier, Inc. · Apr 2010
VENTRIO HERNIA PATCH
K100229 · C.R. Bard, Inc. · Apr 2010