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METICULY Patient-specific titanium maxillofacial mesh implant

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232889
510(k) Type
Traditional
Applicant
Meticuly Co., Ltd.
Country
Thailand
FDA Decision
Substantially Equivalent
Decision Date
4/30/2024
Days to Decision
225 days
Submission Type
Summary

METICULY Patient-specific titanium maxillofacial mesh implant

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232889
510(k) Type
Traditional
Applicant
Meticuly Co., Ltd.
Country
Thailand
FDA Decision
Substantially Equivalent
Decision Date
4/30/2024
Days to Decision
225 days
Submission Type
Summary