510(k) K870130

DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM by Den-Mat Corp. — Product Code ELR

K870130 is an FDA 510(k) premarket notification submitted by Den-Mat Corp. for the device "DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEM". The FDA issued a decision of Substantially Equivalent on February 19, 1987. The device falls under product code ELR (Post, Root Canal), a Class I device regulated under 21 CFR 872.3810. Den-Mat Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 19, 1987
Date Received
January 12, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Post, Root Canal
Device Class
Class I
Regulation Number
872.3810
Review Panel
DE
Submission Type