510(k) K911905

DEKNATEL(R) MICROFLEX OPHTHAL POLY SUTURE,MODIFIED by Deknatel, Inc. — Product Code GAW

K911905 is an FDA 510(k) premarket notification submitted by Deknatel, Inc. for the device "DEKNATEL(R) MICROFLEX OPHTHAL POLY SUTURE,MODIFIED". The FDA issued a decision of Substantially Equivalent on July 2, 1991. The device falls under product code GAW (Suture, Nonabsorbable, Synthetic, Polypropylene), a Class II device regulated under 21 CFR 878.5010. Deknatel, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 2, 1991
Date Received
April 19, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Suture, Nonabsorbable, Synthetic, Polypropylene
Device Class
Class II
Regulation Number
878.5010
Review Panel
SU
Submission Type