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BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K893203
510(k) Type
Traditional
Applicant
KARLIN TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/1990
Days to Decision
343 days

BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K893203
510(k) Type
Traditional
Applicant
KARLIN TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/1990
Days to Decision
343 days