510(k) K896310

ACUFEX FIXATION BUTTON; RETENTION BAR, WEDGE by Acufex Microsurgical, Inc. — Product Code KGS

K896310 is an FDA 510(k) premarket notification submitted by Acufex Microsurgical, Inc. for the device "ACUFEX FIXATION BUTTON; RETENTION BAR, WEDGE". The FDA issued a decision of Substantially Equivalent on November 20, 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
November 20, 1989
Date Received
November 1, 1989
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