Class Class II
Prophecy Surgical Planning System (K241999)
Description
Prophecy Surgical Planning System by Wright Medical Technology, Inc. (Stryker), an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241999
Clearance Date2024-11-01
Clearance TypeTraditional
Product CodeHSN
Regulation Number888.3110
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241999
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. Prophecy Surgical Planning System (K241999) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K222835 | Prophecy Preoperative Navigation Alignment System | Wrightmedicaltechnologyinc | 2023 |
Trace the full predicate network for K241999
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.