510(k) K942442

ACUFEX T-FIX DELIVERY SYSTEM by Acufex Microsurgical, Inc. — Product Code MIA

K942442 is an FDA 510(k) premarket notification submitted by Acufex Microsurgical, Inc. for the device "ACUFEX T-FIX DELIVERY SYSTEM". The FDA issued a decision of Substantially Equivalent on December 5, 1994. The device falls under product code MIA (Needle, Spinal, Short Term), a Class II device regulated under 21 CFR 868.5150. Acufex Microsurgical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 5, 1994
Date Received
May 23, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Needle, Spinal, Short Term
Device Class
Class II
Regulation Number
868.5150
Review Panel
AN
Submission Type