Cleared Traditional

OPTIME, SINUSORB PGA

K062366 · Peters Surgical · General & Plastic Surgery
Oct 2006
Decision
49d
Days
Class 2
Risk

About This 510(k) Submission

K062366 is an FDA 510(k) clearance for the OPTIME, SINUSORB PGA, a Suture, Absorbable, Synthetic, Polyglycolic Acid (Class II — Special Controls, product code GAM), submitted by Peters Surgical (Bobigny Cedex, FR). The FDA issued a Cleared decision on October 2, 2006, 49 days after receiving the submission on August 14, 2006. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4493.

Submission Details

510(k) Number K062366 FDA.gov
FDA Decision Cleared SESE
Date Received August 14, 2006
Decision Date October 02, 2006
Days to Decision 49 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code GAM — Suture, Absorbable, Synthetic, Polyglycolic Acid
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.4493

Similar Devices — GAM Suture, Absorbable, Synthetic, Polyglycolic Acid

All 146
MONOCRYL? Plus Antibacterial Poliglecaprone ? 25 (Monofilament), Sterile Synthetic Absorbable Surgical Suture
K253852 · Ethicon, Inc. · Feb 2026
STRATAFIX? Spiral PDS? Plus Knotless Tissue Control Device; STRATAFIX? Spiral MONOCRYL? Plus Knotless Tissue Control Device
K252743 · Ethicon, Inc. · Dec 2025
TroClose 1200
K253620 · Gordian Surgical, Ltd. · Dec 2025
PGLA90 Poly(glycolide-co-L-lactide) Surgical Sutures (Calypso); PGLA90 Poly(glycolide-co-L-lactide) Surgical Sutures (Odysseus)
K252820 · Internacional Farmac?utica S.A DE C.V · Oct 2025
Monotime and Optime R
K233265 · Peters Surgical · Oct 2024
Peters Surgical ADVANTIME Absorbable Suture (ADVANTIME)
K232372 · Peters Surgical · Jul 2024