510(k) K872608

HEWSON A.C.L. GUIDE SET by Concept, Inc. — Product Code KGS

K872608 is an FDA 510(k) premarket notification submitted by Concept, Inc. for the device "HEWSON A.C.L. GUIDE SET". The FDA issued a decision of Substantially Equivalent on September 16, 1987. The device falls under product code KGS (Retention Device, Suture), a Class I device regulated under 21 CFR 878.4930. Concept, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 16, 1987
Date Received
July 6, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Retention Device, Suture
Device Class
Class I
Regulation Number
878.4930
Review Panel
SU
Submission Type