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FS 1000 KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991052
510(k) Type
Traditional
Applicant
RENAISSANCE INSTRUMENTS, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/1999
Days to Decision
225 days
Submission Type
Statement

FS 1000 KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991052
510(k) Type
Traditional
Applicant
RENAISSANCE INSTRUMENTS, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/1999
Days to Decision
225 days
Submission Type
Statement