Company ยท US
Cohort Medical Products Group, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 1997. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Feb 24, 1997 | K964975 | COHORT DISCECTOMY SYSTEMS (CDS) Cohort Medical Products Group, Inc. | HRX |
| Nov 6, 1995 | K950011 | COHORT(TM) ANTERIOR PLATE SYSTEM (APS) Cohort Medical Products Group, Inc. | KWQ |
| Dec 8, 1994 | K943804 | BONE SCREW Cohort Medical Products Group, Inc. | HWC |
| Oct 20, 1994 | K943472 | COHORT AVB RETRACTOR SYSTEM Cohort Medical Products Group, Inc. | HXB |
| Oct 14, 1994 | K943474 | CANNULATED BONE SCREW Cohort Medical Products Group, Inc. | HWC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||