Minisling Adjustable Polymer Sling & Surgical Mesh with Self-Anchoring System

FDA 510(k) K070846 · Prosurg, Inc.

Substantially Equivalent

510(k) numberK070846

Submission

Device name
Minisling Adjustable Polymer Sling & Surgical Mesh with Self-Anchoring System
Applicant
Prosurg, Inc.
San Jose, CA, US
Received
March 28, 2007
Decision date
July 2, 2007
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FTL – Mesh, Surgical, Polymeric
Device class
Class II (moderate risk)
Regulation
21 CFR 878.3300
Specialty
General, Plastic Surgery
Implant
Yes

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Questions and answers

When was Minisling Adjustable Polymer Sling & Surgical Mesh with Self-Anchoring System cleared by the FDA?

Minisling Adjustable Polymer Sling & Surgical Mesh with Self-Anchoring System (K070846) received a 510(k) decision of Substantially Equivalent on July 2, 2007, 96 days after the submission was received.

What is the product code of K070846?

The FDA product code is FTL – Mesh, Surgical, Polymeric, a Class II (moderate risk) device regulated under 21 CFR 878.3300.