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FRACTURE RISK ASSESSMENT FOR THE NORLAND SXA 3000 BONE DENSITOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980289
510(k) Type
Traditional
Applicant
NORLAND CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/1998
Days to Decision
137 days
Submission Type
Summary

FRACTURE RISK ASSESSMENT FOR THE NORLAND SXA 3000 BONE DENSITOMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980289
510(k) Type
Traditional
Applicant
NORLAND CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/1998
Days to Decision
137 days
Submission Type
Summary