Iss Offset Heads

FDA 510(k) K003428 · Biomet, Inc.

Substantially Equivalent

510(k) numberK003428

Submission

Device name
Iss Offset Heads
Applicant
Biomet, Inc.
Warsaw, IN, US
Received
November 3, 2000
Decision date
November 24, 2000
Decision
Substantially Equivalent (SESE)
Type
Special 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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K161782Arthrex Univers Revers Shoulder Prosthesis SystemHSD · Traditional Arthrex, Inc.11/21/2016SE
K161620Anatomical Shoulder Domelock Dome centricHSD · Traditional Zimmer GmbH11/01/2016SE
K151527Arthrex Univers Revers CA Heads and AdaptersHSD · Traditional Arthrex, Inc.04/19/2016SE
K142942HemiCAP Humeral Head XL (HHXL) Articular Resurfacing SystemHSD · Special Arthrosurface, Inc.12/19/2014SE
K131298Exactech Equinoxe Resurfacing Humeral Head SystemHSD · Traditional Exactech, Inc.11/26/2013SE

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K213287StageOne Knee Cement Spacer MoldsMBB · Traditional 09/02/2022SE
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K212435Comprehensive Humeral Fracture Positioning SleevesKWS · Traditional 12/10/2021SE
K210192A.L.P.S. Clavicle Plating SystemHRS · Special 02/19/2021SE
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Questions and answers

When was Iss Offset Heads cleared by the FDA?

Iss Offset Heads (K003428) received a 510(k) decision of Substantially Equivalent on November 24, 2000, 21 days after the submission was received.

What is the product code of K003428?

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