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Stryker Cutomized Mandible Recon Plate; Stryker Surgeon iD Mandible Recon Plate

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222650
510(k) Type
Traditional
Applicant
Stryker Craniomaxillofacial (Cmf)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2022
Days to Decision
99 days
Submission Type
Summary

Stryker Cutomized Mandible Recon Plate; Stryker Surgeon iD Mandible Recon Plate

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222650
510(k) Type
Traditional
Applicant
Stryker Craniomaxillofacial (Cmf)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2022
Days to Decision
99 days
Submission Type
Summary