510(k) K233203

Device
Soft Tissue Augmentation Resorbable Matrix
Applicant
Collagen Matrix, Inc.
510(k) number
K233203
Product code
NPL
Decision
Substantially Equivalent (SESE)
Decision date
2024-05-01
Date received
2023-09-28
Regulation
872.3930
Classification name
Barrier, Animal Source, Intraoral
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Daniel Fernandez
Address
15 Thornton Rd. Oakland NJ US 07436 07436

FDA Registration Numbers

Source Documents

510(k) summary PDF

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