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INTEGRA ELECTRODE TUNNELING NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K102802
510(k) Type
Traditional
Applicant
INTEGRA LIFESCIENCES CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2010
Days to Decision
57 days
Submission Type
Summary

INTEGRA ELECTRODE TUNNELING NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K102802
510(k) Type
Traditional
Applicant
INTEGRA LIFESCIENCES CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/2010
Days to Decision
57 days
Submission Type
Summary