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Neoss Individual Prosthetics

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211396
510(k) Type
Traditional
Applicant
Neoss Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/17/2022
Days to Decision
377 days
Submission Type
Summary

Neoss Individual Prosthetics

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211396
510(k) Type
Traditional
Applicant
Neoss Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
5/17/2022
Days to Decision
377 days
Submission Type
Summary