Last synced on 25 April 2025 at 11:05 pm

COHORT(TM) ANTERIOR PLATE SYSTEM (APS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950011
510(k) Type
Traditional
Applicant
COHORT MEDICAL PRODUCTS GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/6/1995
Days to Decision
307 days
Submission Type
Statement

COHORT(TM) ANTERIOR PLATE SYSTEM (APS)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950011
510(k) Type
Traditional
Applicant
COHORT MEDICAL PRODUCTS GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/6/1995
Days to Decision
307 days
Submission Type
Statement