510(k) K131947

PROVOX VEGA PUNCTURE SET by Atos Medical AB — Product Code EWL

K131947 is an FDA 510(k) premarket notification submitted by Atos Medical AB for the device "PROVOX VEGA PUNCTURE SET". The FDA issued a decision of Substantially Equivalent on October 18, 2013. The device falls under product code EWL (Prosthesis, Laryngeal (Taub)), a Class II device regulated under 21 CFR 874.3730. Atos Medical AB has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 18, 2013
Date Received
June 27, 2013
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Laryngeal (Taub)
Device Class
Class II
Regulation Number
874.3730
Review Panel
EN
Submission Type