510(k) K873649

FLEX GOLD by Flexmedics — Product Code EJF

K873649 is an FDA 510(k) premarket notification submitted by Flexmedics for the device "FLEX GOLD". The FDA issued a decision of Substantially Equivalent on October 5, 1987. The device falls under product code EJF (Bracket, Metal, Orthodontic), a Class I device regulated under 21 CFR 872.5410. Flexmedics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 5, 1987
Date Received
September 9, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bracket, Metal, Orthodontic
Device Class
Class I
Regulation Number
872.5410
Review Panel
DE
Submission Type