510(k) K910456

ZARA CHIN IMPLANT by Byron Medical — Product Code FWP

K910456 is an FDA 510(k) premarket notification submitted by Byron Medical for the device "ZARA CHIN IMPLANT". The FDA issued a decision of Substantially Equivalent on February 19, 1991. The device falls under product code FWP (Prosthesis, Chin, Internal), a Class II device regulated under 21 CFR 878.3550. Byron Medical has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 19, 1991
Date Received
February 4, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Chin, Internal
Device Class
Class II
Regulation Number
878.3550
Review Panel
SU
Submission Type