Last synced on 18 April 2025 at 11:05 pm

Scorpio Universal Dome Patella; Scorpio Total Stabilizer Insert; Scorpio-Flex Posterior Stabilized Tibial Insert; Scorpio-Flex Cruciate Retaining Tibial Insert; Scorpio NRG Tibial Bearing Insert – Cruciate Retaining Insert; Scorpio NRG Tibial Bearing Insert – Posteriorly Stabilized Insert

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243817
510(k) Type
Traditional
Applicant
Howmedica Osteonics Corp. dba Stryker Orthopaedics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/2025
Days to Decision
56 days
Submission Type
Summary

Scorpio Universal Dome Patella; Scorpio Total Stabilizer Insert; Scorpio-Flex Posterior Stabilized Tibial Insert; Scorpio-Flex Cruciate Retaining Tibial Insert; Scorpio NRG Tibial Bearing Insert – Cruciate Retaining Insert; Scorpio NRG Tibial Bearing Insert – Posteriorly Stabilized Insert

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243817
510(k) Type
Traditional
Applicant
Howmedica Osteonics Corp. dba Stryker Orthopaedics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/2025
Days to Decision
56 days
Submission Type
Summary