510(k) K761206

INTEROSSEOUS NEEDLE by Smith & Nephew, Mpl Division — Product Code DZM

K761206 is an FDA 510(k) premarket notification submitted by Smith & Nephew, Mpl Division for the device "INTEROSSEOUS NEEDLE". The FDA issued a decision of Substantially Equivalent on December 13, 1976. The device falls under product code DZM (Needle, Dental), a Class I device regulated under 21 CFR 872.4730. Smith & Nephew, Mpl Division has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 13, 1976
Date Received
December 7, 1976
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Dental
Device Class
Class I
Regulation Number
872.4730
Review Panel
DE
Submission Type