Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K962261
Device Classification Name
Implant, Malar
More FDA Info for this Device
510(K) Number
K962261
Device Name
Implant, Malar
Applicant
IMPLANTECH ASSOCIATES, INC.
1730 PENNSYLVANIA AVENUE, NW
WASHINGTON, DC 20006 US
Other 510(k) Applications for this Company
Contact
EDWARD M BASILE
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
LZK
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
06/12/1996
Decision Date
08/19/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact