Triathlon Posterior Stabilized Femoral Component - beaded with Peri-Apatite, Triathlon Cruciate Retaining Femoral Component - beaded with Peri-Apatite

FDA 510(k) K200782 · Howmedica Osteonics Corp.

Substantially Equivalent

510(k) numberK200782

Submission

Device name
Triathlon Posterior Stabilized Femoral Component - beaded with Peri-Apatite, Triathlon Cruciate Retaining Femoral Component - beaded with Peri-Apatite
Applicant
Howmedica Osteonics Corp.
Mahwah, NJ, US
Received
March 26, 2020
Decision date
May 13, 2020
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MBH – Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3565
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was Triathlon Posterior Stabilized Femoral Component - beaded with Peri-Apatite, Triathlon Cruciate Retaining Femoral Component - beaded with Peri-Apatite cleared by the FDA?

Triathlon Posterior Stabilized Femoral Component - beaded with Peri-Apatite, Triathlon Cruciate Retaining Femoral Component - beaded with Peri-Apatite (K200782) received a 510(k) decision of Substantially Equivalent on May 13, 2020, 48 days after the submission was received.

What is the product code of K200782?

The FDA product code is MBH – Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer, a Class II (moderate risk) device regulated under 21 CFR 888.3565.