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PELVIS BELLYBOARD PLUS PATIENT POSITIONING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K040773
510(k) Type
Traditional
Applicant
BIONIX DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2004
Days to Decision
14 days
Submission Type
Summary

PELVIS BELLYBOARD PLUS PATIENT POSITIONING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K040773
510(k) Type
Traditional
Applicant
BIONIX DEVELOPMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2004
Days to Decision
14 days
Submission Type
Summary