Zimmer Trabecular Metal Humeral Stem, Sizes 6MM and 8MM

FDA 510(k) K050761 · Zimmer, Inc.

Substantially Equivalent

510(k) numberK050761

Submission

Device name
Zimmer Trabecular Metal Humeral Stem, Sizes 6MM and 8MM
Applicant
Zimmer, Inc.
Warsaw, IN, US
Received
March 24, 2005
Decision date
April 11, 2005
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KWT – Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3650
Specialty
Orthopedic
Implant
Yes

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Questions and answers

When was Zimmer Trabecular Metal Humeral Stem, Sizes 6MM and 8MM cleared by the FDA?

Zimmer Trabecular Metal Humeral Stem, Sizes 6MM and 8MM (K050761) received a 510(k) decision of Substantially Equivalent on April 11, 2005, 18 days after the submission was received.

What is the product code of K050761?

The FDA product code is KWT – Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented, a Class II (moderate risk) device regulated under 21 CFR 888.3650.