510(k) K252085

Device
Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom)
Applicant
Wright Medical Technology, Inc. (Stryker Corporation)
510(k) number
K252085
Product code
MQV
Decision
Substantially Equivalent (SESE)
Decision date
2025-09-30
Date received
2025-07-02
Regulation
888.3045
Classification name
Filler, Bone Void, Calcium Compound
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Alayne Melancon
Address
1023 Cherry Rd. Memphis TN US 38117 38117

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code MQV

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K250141Synthecure Synthetic Calcium SulfateAustin Medical Ventures, Inc.2025-05-16
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K250556Porous Biologic ScaffoldVentris Medical2025-03-21
K250346BonVie+Elute, Inc.2025-02-26
K241555Moldable Bone Void Filler and Moldable Bone Void Filler + CCCRti Surgical, Inc.2025-02-21
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