510(k) K131853

MENTOR MEMORYSHAPE RESTERILIZABLE GEL SIZER by Mentor Worldwide, LLC — Product Code MRD

K131853 is an FDA 510(k) premarket notification submitted by Mentor Worldwide, LLC for the device "MENTOR MEMORYSHAPE RESTERILIZABLE GEL SIZER". The FDA issued a decision of Substantially Equivalent on July 17, 2013. 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
July 17, 2013
Date Received
June 21, 2013
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

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