Cleared Traditional

K110600 - COLLAGEN DENTAL MAMBRANE - PORCINE TYPE I COLLAGEN

K110600 is an FDA 510(k) clearance for COLLAGEN DENTAL MAMBRANE - PORCINE TYPE..., manufactured by Collagen Matrix, Inc.. The device is a Class 2 Dental device with product code NPL cleared through the Traditional 510(k) pathway after a 149-day FDA review.

K110600 · Collagen Matrix, Inc. · Dental device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Jul 2011
Decision
149d
Days
Class 2
Risk

K110600 is an FDA 510(k) clearance for the COLLAGEN DENTAL MAMBRANE - PORCINE TYPE I COLLAGEN. Classified as Barrier, Animal Source, Intraoral (product code NPL), Class II - Special Controls.

Submitted by Collagen Matrix, Inc. (Oakland, US). The FDA issued a Cleared decision on July 29, 2011 after a review of 149 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3930 - the FDA dental device regulatory 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 Dental review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K110600

510(k) Number K110600 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 02, 2011
Decision Date July 29, 2011
Days to Decision 149 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
21d slower than avg
Panel avg: 128d · This submission: 149d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

NPL Device Classification - Class 2, Special Controls

Product Code NPL Barrier, Animal Source, Intraoral
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3930
Definition An Animal Source Dental Barrier Is An Animal-derived Material Device, Such As Collagen, Intended To Aid In Guided Tissue/bone Regeneration Procedures And To Act As A Stable Barrier For The Containment Of Bone Graft Materials When Placed Around Implants.
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 Dental devices follow this clearance model.

Regulatory Peers - NPL Barrier, Animal Source, Intraoral

All 57
Devices cleared under the same product code (NPL) and FDA review panel - the closest regulatory comparables to K110600.
MESOTHELIUM DENTAL MEMBRANE
K121310 · Kensey Nash Corporation · Jul 2013
COLLADENTAL BARRIER
K100695 · Collamatrix, Inc. · Jan 2013
COVAMAX RESORBABLE COLLAGEN MEMBRANE
K103087 · Biom'Up Sas · Aug 2011
VITALA NATURAL RESORBABLE COLLAGEN MEMBRANE
K101453 · Obi Biologics, Inc. · Jul 2011
GENOSS COLLAGEN MEMBRANE MODEL GCM1020, GCM3040 TOTAL 6 MODELS
K102307 · Genoss Co., Ltd. · May 2011
MUCOGRAFT
K102531 · Ed. Geistlich Soehne AG Fur Chemische Industrie · Nov 2010
K110600 · COLLAGEN DENTAL MAMBRANE - PORCINE TYPE I COLLAGEN
Download PDF FDA Summary Collagen Matrix, Inc.