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TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032238
510(k) Type
Traditional
Applicant
NEUROSEL (MEDICAL) LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/9/2003
Days to Decision
50 days
Submission Type
Summary

TWISTER SUPERELASTIC LIGATING CLIP AND APPLIER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032238
510(k) Type
Traditional
Applicant
NEUROSEL (MEDICAL) LIMITED
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
9/9/2003
Days to Decision
50 days
Submission Type
Summary