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INNOVASIVE DEVICES MENISCAL DART REPAIR SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981340
510(k) Type
Traditional
Applicant
Innovasive Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1998
Days to Decision
70 days
Submission Type
Summary

INNOVASIVE DEVICES MENISCAL DART REPAIR SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981340
510(k) Type
Traditional
Applicant
Innovasive Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/1998
Days to Decision
70 days
Submission Type
Summary