510(k) K253202
- Device
- Hoffmann LRF System
- Applicant
- Stryker GmbH
- 510(k) number
- K253202
- Product code
- KTT
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2025-12-19
- Date received
- 2025-09-26
- Regulation
- 888.3030
- Classification name
- Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- N
- Source
- FDA openFDA 510(k) dataset plus migrated FDA.report data
Related Records
Applicant Contact
- Contact
- Amy Noccioli
- Address
- Bohnackerweg 1 Selzach CH
FDA Registration Numbers
- 3015709929
- 1423662
- 1450662
- 2031910
- 9680619
- 1226074
- 3023808054
- 1649390
- 3009540749
- 3004176895
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- 1528668
- 3014302784
Source Documents
FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON
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