510(k) K884565

ACUFEX FIXATION BUTTON by Acufex Microsurgical, Inc. — Product Code KGS

K884565 is an FDA 510(k) premarket notification submitted by Acufex Microsurgical, Inc. for the device "ACUFEX FIXATION BUTTON". The FDA issued a decision of Substantially Equivalent on February 27, 1989. The device falls under product code KGS (Retention Device, Suture), a Class I device regulated under 21 CFR 878.4930. Acufex Microsurgical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 27, 1989
Date Received
November 1, 1988
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