SURGITEK SIZER FOR PENILE PROSTHESIS

K830917 · Medical Engineering Corp. · FAE · Apr 12, 1983 · Gastroenterology, Urology

Device Facts

Record IDK830917
Device NameSURGITEK SIZER FOR PENILE PROSTHESIS
ApplicantMedical Engineering Corp.
Product CodeFAE · Gastroenterology, Urology
Decision DateApr 12, 1983
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 876.3630
Device ClassClass 2

Regulatory Classification

Identification

A penile rigidity implant is a device that consists of a pair of semi-rigid rods implanted in the corpora cavernosa of the penis to provide rigidity. It is intended to be used in men diagnosed as having erectile dysfunction.

Special Controls

The special control for this device is the FDA guidance entitled “Guidance for the Content of Premarket Notifications for Penile Rigidity Implants.”

Innolitics

Panel 1

/
Sort by
Ready

Predicate graph will load when search results are available.

Embedding visualization will load when search results are available.

PDF viewer will load when search results are available.

Loading panels...

Select an item from the tree

Click any panel, subpart, regulation, product code, or device to see details here.

Section Matches

Results will appear here.

Product Code Matches

Results will appear here.

Special Control Matches

Results will appear here.

Loading collections...