Class Class II
CREED™ Cannulated Screws (K223847)
Description
CREED™ Cannulated Screws by Glw, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK223847
Clearance Date2023-01-25
Clearance TypeSpecial
Product CodeHWC
Regulation Number888.3040
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K223847
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. CREED™ Cannulated Screws (K223847) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K200291 | CREED™ Cannulated Screws | Glw Medical, Inc. | 2020 |
Trace the full predicate network for K223847
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.