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LOTUS ULTRASONIC SYSTEM FOR CEMENTED IMPLANT EXTRACTION (USCIX)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072961
510(k) Type
Traditional
Applicant
SRA DEVELOPMENTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/19/2007
Days to Decision
61 days
Submission Type
Summary

LOTUS ULTRASONIC SYSTEM FOR CEMENTED IMPLANT EXTRACTION (USCIX)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072961
510(k) Type
Traditional
Applicant
SRA DEVELOPMENTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/19/2007
Days to Decision
61 days
Submission Type
Summary