Medpor Surg Implant Material:Prefor Cran/Fac Impla

FDA 510(k) K922489 · Porex Technologies Corp.

Substantially Equivalent

510(k) numberK922489

Submission

Device name
Medpor Surg Implant Material:Prefor Cran/Fac Impla
Applicant
Porex Technologies Corp.
Fairburn, GA, US
Received
May 27, 1992
Decision date
September 2, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FWP – Prosthesis, Chin, Internal
Device class
Class II (moderate risk)
Regulation
21 CFR 878.3550
Specialty
General, Plastic Surgery
Implant
Yes

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Questions and answers

When was Medpor Surg Implant Material:Prefor Cran/Fac Impla cleared by the FDA?

Medpor Surg Implant Material:Prefor Cran/Fac Impla (K922489) received a 510(k) decision of Substantially Equivalent on September 2, 1992, 98 days after the submission was received.

What is the product code of K922489?

The FDA product code is FWP – Prosthesis, Chin, Internal, a Class II (moderate risk) device regulated under 21 CFR 878.3550.