Cleared Traditional

K182074 - Mineral Collagen Composite Bioactive Mo...

K182074 is the FDA 510(k) clearance for Mineral Collagen Composite Bioactive Mo... by Collagen Matrix, Inc.. It is a Class 2 Orthopedic device (product code MQV) cleared through the Traditional 510(k) pathway after a 232-day FDA review.

K182074 · Collagen Matrix, Inc. · Orthopedic device
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Mar 2019
Decision
232d
Days
Class 2
Risk

K182074 is an FDA 510(k) clearance for the Mineral Collagen Composite Bioactive Moldable. Classified as Filler, Bone Void, Calcium Compound (product code MQV), Class II - Special Controls.

Submitted by Collagen Matrix, Inc. (Oakland, US). The FDA issued a Cleared decision on March 21, 2019 after a review of 232 days - an extended review cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3045 - the FDA orthopedic 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 Orthopedic review framework, consistent with the majority of Class II 510(k) submissions.

View all Collagen Matrix, Inc. devices

Submission Details

510(k) Number K182074 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 01, 2018
Decision Date March 21, 2019
Days to Decision 232 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
110d slower than avg
Panel avg: 122d · This submission: 232d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code MQV Filler, Bone Void, Calcium Compound
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3045
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 Orthopedic devices follow this clearance model.

Regulatory Peers - MQV Filler, Bone Void, Calcium Compound

All 232
Devices cleared under the same product code (MQV) and FDA review panel - the closest regulatory comparables to K182074.
AccuFill Bone Substitute Material
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K190110 · Artoss GmbH · Apr 2019
PROSTIM Injectable Inductive Graft
K190283 · Wrightmedicaltechnologyinc · Mar 2019
FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute
K182670 · Prosidyan, Inc. · Dec 2018
MagnetOs Putty
K181958 · Kuros Biosciences B.V · Dec 2018