510(k) K241552

MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer by Mentor Worldwide, LLC — Product Code MRD

K241552 is an FDA 510(k) premarket notification submitted by Mentor Worldwide, LLC for the device "MENTOR™ MemoryGel™ Enhance Single Use Gel Sizer". The FDA issued a decision of Substantially Equivalent on September 6, 2024. The device falls under product code MRD (Mammary Sizer), a Class U device. Mentor Worldwide, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 6, 2024
Date Received
May 31, 2024
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mammary Sizer
Device Class
Class U
Regulation Number
Review Panel
SU
Submission Type