Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K021782
Device Classification Name
Nail, Fixation, Bone
More FDA Info for this Device
510(K) Number
K021782
Device Name
Nail, Fixation, Bone
Applicant
AAP IMPLANTATE AG
LORENZWEG 5
BERLIN 12099 DE
Other 510(k) Applications for this Company
Contact
DIPL-ING CHRISTIAN ABEL
Other 510(k) Applications for this Contact
Regulation Number
888.3030
More FDA Info for this Regulation Number
Classification Product Code
JDS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/30/2002
Decision Date
08/26/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact