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FRACTURE RISK ASSESSMENT FOR THE NORLAND SXA 3000 BONE DENSITOMETER

Page Type
Cleared 510(K)
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)
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