510(k) K863742

FLEXMEDICS NITINOL ARCH WIRE by Flexmedics — Product Code DZC

K863742 is an FDA 510(k) premarket notification submitted by Flexmedics for the device "FLEXMEDICS NITINOL ARCH WIRE". The FDA issued a decision of Substantially Equivalent on November 24, 1986. The device falls under product code DZC (Wire, 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
November 24, 1986
Date Received
September 23, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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