510(k) K801073

STRAITH CHIN IMPLANTS by Surgical Technology Laboratories, Inc. — Product Code FWP

K801073 is an FDA 510(k) premarket notification submitted by Surgical Technology Laboratories, Inc. for the device "STRAITH CHIN IMPLANTS". The FDA issued a decision of Substantially Equivalent on May 20, 1980. The device falls under product code FWP (Prosthesis, Chin, Internal), a Class II device regulated under 21 CFR 878.3550. Surgical Technology Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 20, 1980
Date Received
May 6, 1980
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