510(k) K203495

Device
Arthrex SwiveLock Anchor
Applicant
Arthrex, Inc.
510(k) number
K203495
Product code
MAI
Decision
Substantially Equivalent (SESE)
Decision date
2021-04-19
Date received
2020-11-27
Regulation
888.3030
Classification name
Fastener, Fixation, Biodegradable, Soft Tissue
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Kelsey Roberts
Address
1370 Creekside Blvd. Naples FL US 34108 34108

FDA Registration Numbers

Source Documents

510(k) summary PDF

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