Arthrocare Arthroscopic Electrosurgery System (Model 970)

510(k) Number

K961747 ↗

FDA Product Code

HRX

Regulation

21 CFR Part 888.1100

Advisory Committee

Orthopedic

FDA Decision

SESE Substantially Equivalent

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  FDA 510(k) K000511 Active Cleared 13 Mar 2000

See all devices from ArthroCare Corporation →