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Encore Shoulder Primary Humeral Stem (500-00 +2 more)

FDA 510(k)

Class II (US FDA 510(k))

510(k) K080402

by Encore Medical L.P.

Identifiers

510(k) Number
K080402 FDA 510(k)
FDA Product Code
KWS FDA 510(k)
Models / Variants
500-00 FDA 510(k)
Model 520-38 FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 888.3660 FDA 510(k)
Regulation Number
888.3660 FDA 510(k)
Advisory Committee
Orthopedic FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Encore Shoulder Primary Humeral Stem (500-00 +2 more) by Encore Medical L.P. — Class II — FDA_510K — listed in FDA 510(k) — 3 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Encore Medical L.P.

Sources (1)

  • FDA 510(k) K080402 24 fields · synced Jun 18, 2026