Carticept Medical, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Carticept Medical, Inc.” (first 2011, latest 2015), across 1 product code in 1 review panel. Median 510(k) review time under this name: 82 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 2 | 60 |
| 2013 | 1 | 72 |
| 2014 | 0 | — |
| 2015 | 1 | 232 |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| FRN | Pump, Infusion | 6 | 6 |
Review panels
- General Hospital (6)
Most recent Carticept Medical, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K151255 | Navigator Aesthetic Delivery System | FRN | 2015-12-30 | 232 |
| K124053 | NAVIGATOR DELIVERY SYSTEM (NAVIGATOR DS) | FRN | 2013-03-13 | 72 |
| K122215 | NAVIGATOR DELIVERY SYSTEM (NAVIGATOR DS) | FRN | 2012-10-26 | 93 |
| K120830 | NAVIGATOR DELIVERY SYSTEM (NAVIGATOR DS) | FRN | 2012-04-16 | 28 |
| K112067 | NAVIGATOR DELIVERY SYSTEM (NAVIGATOR DS) | FRN | 2011-09-16 | 59 |
| K101194 | NAVIGATOR DELIVERY SYSTEM (OR NAVIGATOR DS) MODEL: NAV-010 | FRN | 2011-07-11 | 439 |
Recalls
openFDA lists no recalls under a recalling firm named Carticept Medical, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Related HCPCS codes
HCPCS Level II codes whose descriptors match the device names of the product codes filed under Carticept Medical, Inc. (a text match, not an official crosswalk):
- A4220 — Refill kit for implantable infusion pump (via FRN)
- E0786 — Implantable programmable infusion pump, replacement (excludes implantable intraspinal catheter) (via FRN)
- E0785 — Implantable intraspinal (epidural/intrathecal) catheter used with implantable infusion pump, replacement (via FRN)
Frequently asked questions
How many FDA 510(k) clearances are listed under Carticept Medical, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Carticept Medical, Inc.” (first 2011, latest 2015), across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Carticept Medical, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Carticept Medical, Inc. is 82 days.
Which FDA product codes appear under Carticept Medical, Inc.?
The most frequent FDA product codes under this applicant name are FRN (Pump, Infusion, 6).
Next steps
- See all 6 Carticept Medical, Inc. clearances with predicates and recalls
- Run predicate analysis for product code FRN, Carticept Medical, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.