510(k) K980446

SPECTRUM DESIGNS ANTERIOR CHIN IMPLANT by Spectrum Designs, Inc. — Product Code FWP

K980446 is an FDA 510(k) premarket notification submitted by Spectrum Designs, Inc. for the device "SPECTRUM DESIGNS ANTERIOR CHIN IMPLANT". The FDA issued a decision of Substantially Equivalent on May 6, 1998. The device falls under product code FWP (Prosthesis, Chin, Internal), a Class II device regulated under 21 CFR 878.3550. Spectrum Designs, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 6, 1998
Date Received
February 5, 1998
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