Atlas FDA

RibPlate System

FDA 510(k) clearance K261054 · decided 2026-07-01

Clearance details

K-number
K261054
Device name
RibPlate System
Applicant
Stryker Leibinger GmbH & Co KG
Decision
Substantially Equivalent
Date received
2026-03-31
Decision date
2026-07-01
Days to decision
92 days
Clearance type
Traditional
Product code
HRS
Device class
2
Regulation number
888.3030
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Freiburg, DE
Third-party review
No
Expedited review
No

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RecordFirmDate
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APTUS Clavicle System 2.8 (K260761)Medartis AG2026-06-05
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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
Adherus AutoSpray Dural Sealant (P130014/S021)Stryker Leibinger GmbH & Co KG2025-11-06
TMJ Concepts Patient Fitted Temporomandibular Joint (TMJ) Reconstruction Prosthesis System (P980052/S016)Stryker Leibinger, GmbH & Co KG2025-07-23
Adherus AutoSpray Dural Sealant, Adherus AutoSpray ET Dural Sealant (P130014/S020)Stryker Leibinger GmbH & Co KG2024-08-29
TMJ Concepts Patient-Fitted TMJ Reconstruction Prosthesis (P980052/S015)Stryker Leibinger, GmbH & Co KG2024-08-08
TMJ Concepts Patient-Fitted TMJ Reconstruction Prosthesis (P980052/S014)Stryker Leibinger, GmbH & Co KG2024-07-30
Adherus AutoSpray Dural Sealant, Adherus AutoSpray ET Dural Sealant (P130014/S019)Stryker Leibinger GmbH & Co KG2023-10-07
Adherus AutoSpray Dural Sealant, Adherus AutoSpray ET Dural Sealant (P130014/S018)Stryker Leibinger GmbH & Co KG2023-08-25
TMJ Concepts Patient-Fitted Temporomandibular Joint (TMJ) st (P980052/S012)Stryker Leibinger, GmbH & Co KG2023-08-22