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CRADLE FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K941772
510(k) Type
Traditional
Applicant
NEOLIGAMENTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/7/1995
Days to Decision
483 days
Submission Type
Statement

CRADLE FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K941772
510(k) Type
Traditional
Applicant
NEOLIGAMENTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/7/1995
Days to Decision
483 days
Submission Type
Statement