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HA-TI (HAND-TITANIUM SCREW) IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901927
510(k) Type
Traditional
Applicant
MATHYS CORP. OF NORTH AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1991
Days to Decision
249 days

HA-TI (HAND-TITANIUM SCREW) IMPLANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K901927
510(k) Type
Traditional
Applicant
MATHYS CORP. OF NORTH AMERICA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1991
Days to Decision
249 days