Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid (K241491)
Description
Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid by Stryker Corporation (Tornier, S.A.S.), an FDA 510(k) cleared orthopedic device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241491
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. Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid (K241491) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K232265 | BLUEPRINT™ Patient Specific Instrumentation | Tornier S.A.S. | 2024 |
| K211359 | Tornier Perform™ Patient-Matched Primary Reversed Glenoid a... | Tornier, Inc. | 2021 |
Trace the full predicate network for K241491
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.