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TEW CRANIAL/SPINAL RETRACTOR MODEL A1090

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960807
510(k) Type
Traditional
Applicant
OHIO MEDICAL INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/1996
Days to Decision
79 days
Submission Type
Summary

TEW CRANIAL/SPINAL RETRACTOR MODEL A1090

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960807
510(k) Type
Traditional
Applicant
OHIO MEDICAL INSTRUMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/1996
Days to Decision
79 days
Submission Type
Summary