510(k) K213644

Arthrex Knotless Mini TightRopes by Arthrex, Inc. — Product Code HTN

K213644 is an FDA 510(k) premarket notification submitted by Arthrex, Inc. for the device "Arthrex Knotless Mini TightRopes". The FDA issued a decision of Substantially Equivalent on December 17, 2021. The device falls under product code HTN (Washer, Bolt Nut), a Class II device regulated under 21 CFR 888.3030. Arthrex, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 17, 2021
Date Received
November 18, 2021
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Washer, Bolt Nut
Device Class
Class II
Regulation Number
888.3030
Review Panel
OR
Submission Type