510(k) K253888

Device
MOLLI 2 System
Applicant
Stryker Endoscopy
510(k) number
K253888
Product code
NEU
Decision
Substantially Equivalent (SESE)
Decision date
2025-12-31
Date received
2025-12-04
Regulation
878.4300
Classification name
Marker, Radiographic, Implantable
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Michelle Stephens
Address
5900 Optical Ct. San Jose CA US 95138 95138

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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