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DIRECT BONDED BRACKET REMOVER

Page Type
Cleared 510(K)
510(k) Number
K832301
510(k) Type
Traditional
Applicant
NORTHWEST ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/1983
Days to Decision
49 days

DIRECT BONDED BRACKET REMOVER

Page Type
Cleared 510(K)
510(k) Number
K832301
510(k) Type
Traditional
Applicant
NORTHWEST ORTHOPEDICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/1983
Days to Decision
49 days