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RESCH ARTHROSCOPIC AND PERCUTANEOUS SCREW FIXATION SYSTEM (A.S.F.)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961498
510(k) Type
Traditional
Applicant
HOWMEDICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/1997
Days to Decision
294 days
Submission Type
Summary

RESCH ARTHROSCOPIC AND PERCUTANEOUS SCREW FIXATION SYSTEM (A.S.F.)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961498
510(k) Type
Traditional
Applicant
HOWMEDICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/1997
Days to Decision
294 days
Submission Type
Summary