Depuy Opti-Con and E-Z Shield Systems

FDA 510(k) K964114 · Depuy, Inc.

Substantially Equivalent

510(k) numberK964114

Submission

Device name
Depuy Opti-Con and E-Z Shield Systems
Applicant
Depuy, Inc.
Warsaw, IN, US
Received
October 15, 1996
Decision date
May 6, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FXX – Mask, Surgical
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4040
Specialty
General, Plastic Surgery

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Questions and answers

When was Depuy Opti-Con and E-Z Shield Systems cleared by the FDA?

Depuy Opti-Con and E-Z Shield Systems (K964114) received a 510(k) decision of Substantially Equivalent on May 6, 1997, 203 days after the submission was received.

What is the product code of K964114?

The FDA product code is FXX – Mask, Surgical, a Class II (moderate risk) device regulated under 21 CFR 878.4040.