Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K042573
Device Classification Name
Screw, Fixation, Intraosseous
More FDA Info for this Device
510(K) Number
K042573
Device Name
Screw, Fixation, Intraosseous
Applicant
KLS-MARTIN L.P.
1239-1 ST. JOHN'S IND. PKWY.
SOUTH
JACKSONVILLE, FL 32246 US
Other 510(k) Applications for this Company
Contact
JENNIFER DAMATO
Other 510(k) Applications for this Contact
Regulation Number
872.4880
More FDA Info for this Regulation Number
Classification Product Code
DZL
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/21/2004
Decision Date
10/18/2004
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