510(k) K881274

CENTER BEND ARCH WIRES by Flexmedics — Product Code EJF

K881274 is an FDA 510(k) premarket notification submitted by Flexmedics for the device "CENTER BEND ARCH WIRES". The FDA issued a decision of Substantially Equivalent on April 12, 1988. 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
April 12, 1988
Date Received
March 25, 1988
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