510(k) K952122

V-GNATHOS PLUS by Metalor Dental USA Corp. — Product Code EJT

K952122 is an FDA 510(k) premarket notification submitted by Metalor Dental USA Corp. for the device "V-GNATHOS PLUS". The FDA issued a decision of Substantially Equivalent on June 6, 1995. The device falls under product code EJT (Alloy, Gold-Based Noble Metal), a Class II device regulated under 21 CFR 872.3060. Metalor Dental USA Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 6, 1995
Date Received
May 5, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Alloy, Gold-Based Noble Metal
Device Class
Class II
Regulation Number
872.3060
Review Panel
DE
Submission Type