510(k) K873722

PEDESTAL WALKING HEEL PRODUCT NO. 4183-133 by Martin Medical — Product Code LGF

K873722 is an FDA 510(k) premarket notification submitted by Martin Medical for the device "PEDESTAL WALKING HEEL PRODUCT NO. 4183-133". The FDA issued a decision of Substantially Equivalent on October 2, 1987. The device falls under product code LGF (Component, Cast), a Class I device regulated under 21 CFR 888.5940. Martin Medical has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 2, 1987
Date Received
September 15, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Component, Cast
Device Class
Class I
Regulation Number
888.5940
Review Panel
OR
Submission Type