Cleared Traditional

K073329 - SYGNAL DBM

K073329 is an FDA 510(k) clearance for SYGNAL DBM, manufactured by Musculoskeletal Transplant Foundation. The device is a Class 2 Orthopedic device with product code MBP cleared through the Traditional 510(k) pathway after a 93-day FDA review.

K073329 · Musculoskeletal Transplant Foundation · Orthopedic device
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Optimized for regulatory review, auditing and printing
Feb 2008
Decision
93d
Days
Class 2
Risk

K073329 is an FDA 510(k) clearance for the SYGNAL DBM. Classified as Filler, Bone Void, Osteoinduction (w/o Human Growth Factor) (product code MBP), Class II - Special Controls.

Submitted by Musculoskeletal Transplant Foundation (Edison, US). The FDA issued a Cleared decision on February 28, 2008 after a review of 93 days - within the typical 510(k) review window.

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 Musculoskeletal Transplant Foundation devices

FDA 510(k) Submission Details - K073329

510(k) Number K073329 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 27, 2007
Decision Date February 28, 2008
Days to Decision 93 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
29d faster than avg
Panel avg: 122d · This submission: 93d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MBP Device Classification - Class 2, Special Controls

Product Code MBP Filler, Bone Void, Osteoinduction (w/o Human Growth Factor)
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 - MBP Filler, Bone Void, Osteoinduction (w/o Human Growth Factor)

All 25
Devices cleared under the same product code (MBP) and FDA review panel - the closest regulatory comparables to K073329.
DBX DEMINERALIZED BONE MATRIX PUTTY, DBX DEMINERALIZED BONE MATRIX PASTE
K080399 · Musculoskeletal Transplant Foundation · Oct 2008
SYGNAL DBM
K080405 · Musculoskeletal Transplant Foundation · Aug 2008
CAP PLUS, EQUIVABONE, CAP/DBM
K080329 · Etex Corp. · Apr 2008
OPTECURE
K063685 · Exactech, Inc. · Jun 2007
DBX DEMINERALIZED BONE MATRIX MIX
K063676 · Musculoskeletal Transplant Foundation · Mar 2007
DBX-H HEMOSTATIC DEMINERALIZED BONE MATRIX PUTTY
K061131 · Orthocon, Inc. · Feb 2007