Atlas FDA

FIBER-METAL POST

FDA 510(k) clearance K060075 · decided 2006-03-30

Clearance details

K-number
K060075
Device name
FIBER-METAL POST
Applicant
Foremost Dental, LLC
Decision
Substantially Equivalent
Date received
2006-01-10
Decision date
2006-03-30
Days to decision
79 days
Clearance type
Traditional
Product code
ELR
Device class
1
Regulation number
872.3810
Medical specialty
Dental
Advisory committee
Dental
Location
Ayer, MA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Foremost Dental

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
FRC POSTEC PLUS (K042848)Ivoclar Vivadent, Inc.2004-11-22
EVERSTICK POST (K030820)Stick Tech , Ltd.2003-05-20
FIBIOCORE (K020431)Est. Anthogyr2002-07-03
CARBON POST (K012496)J. Morita USA, Inc.2002-05-17
FRC POSTEC (K013802)Ivoclar Vivadent, Inc.2002-05-01
GLASS POST (K012849)J. Morita USA, Inc.2002-03-27
SNOWPOST, SNOWLIGHT (K012354)Danville Materials, Inc.2001-10-10
HARALD NORDIN GLASSIX GLASS FIBER COMPOSITE DENTAL POST (K003221)Harald Nordin S.A2000-10-25
HARALD NORDIN CARBONITE CARBON FIBER COMPOSITE DENTAL POST (K003219)Harald Nordin S.A2000-10-25
TENAX WHITE POST (K993545)Coltene/Whaledent, Inc.2000-04-14
PARAPOST FIBER WHITE (K000311)Coltene/Whaledent, Inc.2000-03-14
FIBREKOR POST SYSTEM (K983266)Jeneric/Pentron, Inc.1998-11-09

Recalls involving this device

No recalls on record reference this clearance.