510(k) K903643

DEKNATEL MICROFLEX OPHTHALMIC POLYPROPYLENE SUTURE by Deknatel, Inc. — Product Code GAW

K903643 is an FDA 510(k) premarket notification submitted by Deknatel, Inc. for the device "DEKNATEL MICROFLEX OPHTHALMIC POLYPROPYLENE SUTURE". The FDA issued a decision of Substantially Equivalent on December 24, 1990. 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
December 24, 1990
Date Received
August 10, 1990
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