Cleared Traditional

K102788 - TORNIER BIOFIBER SCAFFOLD

K102788 is the FDA 510(k) clearance for TORNIER BIOFIBER SCAFFOLD by Tornier, Inc.. It is a Class 2 General & Plastic Surgery device (product code FTL) cleared through the Traditional 510(k) pathway after a 228-day FDA review.

K102788 · Tornier, Inc. · General & Plastic Surgery device
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May 2011
Decision
228d
Days
Class 2
Risk

K102788 is an FDA 510(k) clearance for the TORNIER BIOFIBER SCAFFOLD. Classified as Mesh, Surgical, Polymeric (product code FTL), Class II - Special Controls.

Submitted by Tornier, Inc. (Beverly, US). The FDA issued a Cleared decision on May 10, 2011 after a review of 228 days - an extended review cycle.

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. Standard predicate reliance. 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 Tornier, Inc. devices

Submission Details

510(k) Number K102788 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 24, 2010
Decision Date May 10, 2011
Days to Decision 228 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
113d slower than avg
Panel avg: 115d · This submission: 228d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 157
Devices cleared under the same product code (FTL) and FDA review panel - the closest regulatory comparables to K102788.
C-QUR RPM MESH
K121070 · Atrium Medical Corp. · Apr 2012
TORNIER COLLAGEN COATED BIOFIBER SCAFFOLD
K111337 · Tornier, Inc. · Jan 2012
RENASYS AB ABOMINAL DRESSING KIT
K112784 · Smith & Nephew, Inc. · Nov 2011
VENTRALIGHT (TM) ST MESH WITH ECHO PS (TM) POSITIONING SYSTEM
K110820 · C.R. Bard, Inc. · Apr 2011
VENTRIO ST HERNIA PATCH
K101920 · C.R. Bard, Inc. · Mar 2011
VENTRALEX ST HERNIA PATCH
K101928 · C.R. Bard, Inc. · Mar 2011