510(k) K880953

ADVANCED SURGICAL 19 & 20 GAUGE DISP. SCLERAL PLUG by Advanced Surgical Products, Inc. — Product Code LXP

K880953 is an FDA 510(k) premarket notification submitted by Advanced Surgical Products, Inc. for the device "ADVANCED SURGICAL 19 & 20 GAUGE DISP. SCLERAL PLUG". The FDA issued a decision of Substantially Equivalent on May 13, 1988. The device falls under product code LXP (Plug, Scleral), a Class II device regulated under 21 CFR 886.4155. Advanced Surgical Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 13, 1988
Date Received
March 7, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Plug, Scleral
Device Class
Class II
Regulation Number
886.4155
Review Panel
OP
Submission Type

Intended to provide temporary closure of a scleral incision during an ophthalmic procedure.