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PDO Max Suture with Dual Needle

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210871
510(k) Type
Traditional
Applicant
PDO MAX, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2021
Days to Decision
268 days
Submission Type
Summary

PDO Max Suture with Dual Needle

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210871
510(k) Type
Traditional
Applicant
PDO MAX, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2021
Days to Decision
268 days
Submission Type
Summary