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BONE SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K943804
510(k) Type
Traditional
Applicant
COHORT MEDICAL PRODUCTS GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/8/1994
Days to Decision
126 days
Submission Type
Statement

BONE SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K943804
510(k) Type
Traditional
Applicant
COHORT MEDICAL PRODUCTS GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/8/1994
Days to Decision
126 days
Submission Type
Statement