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UNIVERSALL DRILL GUIDE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820226
510(k) Type
Traditional
Applicant
ORTHO PARED INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1982
Days to Decision
8 days

UNIVERSALL DRILL GUIDE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820226
510(k) Type
Traditional
Applicant
ORTHO PARED INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1982
Days to Decision
8 days