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DIRECTIONAL BOOT

Page Type
Cleared 510(K)
510(k) Number
K813150
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1981
Days to Decision
26 days

DIRECTIONAL BOOT

Page Type
Cleared 510(K)
510(k) Number
K813150
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1981
Days to Decision
26 days