FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ARTHREX PUSHLOCK ANCHORS

K Number: K101679 · Decision Oct 22, 2010
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
213
Applicant Total
181
Review Days
129

Basic Information

Device Name
ARTHREX PUSHLOCK ANCHORS
K Number
K101679
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ARTHREX, INC.
Date Received
June 15, 2010
Decision Date
October 22, 2010
Product Code
MAI
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MAI Fastener, Fixation, Biodegradable, Soft Tissue

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