Promos Modular Shoulder System

FDA 510(k) K063578 · Plus Orthopedics AG

Substantially Equivalent

510(k) numberK063578

Submission

Device name
Promos Modular Shoulder System
Applicant
Plus Orthopedics AG
Norfolk, MA, US
Received
November 30, 2006
Decision date
March 2, 2007
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HSD – Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3690
Specialty
Orthopedic
Implant
Yes

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More from Exactech, Inc.

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K061362Pigalileo Total Knee Replacement (TKR) SystemHAW · Traditional 10/06/2006SE
K032126Promos ShoulderHSD · Traditional 01/08/2004SE
K033763Modification to Slim Gliding Nail SystemKTT · Special 12/18/2003SE
K032709Modular Plus Hip StemLWJ · Special 09/23/2003SE
K032548Ip-Xs Compression Nail SystemHSB · Traditional 09/10/2003SE
K032215Vks/Tc-Plus Revision KneeJWH · Special 08/08/2003SE
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Questions and answers

When was Promos Modular Shoulder System cleared by the FDA?

Promos Modular Shoulder System (K063578) received a 510(k) decision of Substantially Equivalent on March 2, 2007, 92 days after the submission was received.

What is the product code of K063578?

The FDA product code is HSD – Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented, a Class II (moderate risk) device regulated under 21 CFR 888.3690.