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Cohort Medical Products Group, Inc.

FDA Regulatory Profile

Cohort Medical Products Group, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 24, 1997.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K964975COHORT DISCECTOMY SYSTEMS (CDS)February 24, 1997
K950011COHORT(TM) ANTERIOR PLATE SYSTEM (APS)November 6, 1995
K943804BONE SCREWDecember 8, 1994
K943472COHORT AVB RETRACTOR SYSTEMOctober 20, 1994
K943474CANNULATED BONE SCREWOctober 14, 1994

FDA data resources