Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K973924
Device Classification Name
Plate, Bone
More FDA Info for this Device
510(K) Number
K973924
Device Name
Plate, Bone
Applicant
FRIATEC AG
9229 CRANFORD DR.
POTOMAC, MD 20854 US
Other 510(k) Applications for this Company
Contact
ROBERT J SLOMOFF
Other 510(k) Applications for this Contact
Regulation Number
872.4760
More FDA Info for this Regulation Number
Classification Product Code
JEY
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/15/1997
Decision Date
05/07/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
DE - Dental
Review Advisory Committee
DE - Dental
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact