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FDA 510(k) Applications Submitted by ARTHRONET MEDICAL, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K023777
11/12/2002
ARTHRONET BLACKLINE 2 AND 3 PIECE ARTHROSCOPIC BLADES, MODELS 123, 133, 153, 163, 173 AND 183
ARTHRONET MEDICAL, INC.
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