FDA.report

510(k) K261241

Device
TriMed Compression Screws
Applicant
TriMed, Inc.
510(k) number
K261241
Product code
HWC
Decision
Substantially Equivalent (SESE)
Decision date
2026-05-14
Date received
2026-04-15
Regulation
888.3040
Classification name
Screw, Fixation, Bone
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Annika Lind
Address
27533 Ave. Hopkins Santa Clarita CA US 91355 91355

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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