Stryker CMF Medpor Customized Implant

FDA 510(k) K121315 · Howmedica Osteonics Corp.

Substantially Equivalent

510(k) numberK121315

Submission

Device name
Stryker CMF Medpor Customized Implant
Applicant
Howmedica Osteonics Corp.
Newnan, GA, US
Received
May 2, 2012
Decision date
November 1, 2012
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 Stryker CMF Medpor Customized Implant cleared by the FDA?

Stryker CMF Medpor Customized Implant (K121315) received a 510(k) decision of Substantially Equivalent on November 1, 2012, 183 days after the submission was received.

What is the product code of K121315?

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