Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K981214
Device Classification Name
Bone Grafting Material, Synthetic
More FDA Info for this Device
510(K) Number
K981214
Device Name
Bone Grafting Material, Synthetic
Applicant
CERAMED DENTAL, LLC.
12860 WEST CEDAR DR.,
SUITE 110
LAKEWOOD, CO 80228 US
Other 510(k) Applications for this Company
Contact
MARK BOWERMAN
Other 510(k) Applications for this Contact
Regulation Number
872.3930
More FDA Info for this Regulation Number
Classification Product Code
LYC
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/02/1998
Decision Date
06/26/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact