Novosource, Inc.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Novosource, Inc.” (first 2013, latest 2026), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 124 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 |
|---|---|---|
| 2013 | 2 | 143 |
| 2014 | 2 | 162 |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 1 | 28 |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Novosource, Inc. took a median 28 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 90 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 3 | 3 |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 1 | 1 |
| OQG | Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented | 1 | 1 |
Review panels
- Orthopedic (5)
Most recent Novosource, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K261032 | NovoKnee (SteriKnee) | JWH | 2026-04-27 | 28 |
| K140701 | NOVOHIP BIPOLAR HEAD/NOVOHIP VITAMIN E LINER/ BONE SCREWS/ HOLE PLUG | OQG | 2014-06-27 | 99 |
| K132158 | NOVOHIP TOTAL HIP SYSTEM | LPH | 2014-02-21 | 224 |
| K131398 | NOVOKNEE TOTAL KNEE SYSTEM | JWH | 2013-09-16 | 124 |
| K123339 | TK1 TOTAL KNEE SYSTEM | JWH | 2013-04-11 | 162 |
Recalls
1 product recalls in 1 recall events; 1 initiated in the last five years. Most recent: 2024-09-19.
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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Novosource, Inc.?
FDA lists 5 510(k) clearances under the applicant name “Novosource, Inc.” (first 2013, latest 2026), across 3 product codes 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 Novosource, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Novosource, Inc. is 124 days.
Which FDA product codes appear under Novosource, Inc.?
The most frequent FDA product codes under this applicant name are JWH (Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer, 3); LPH (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented, 1); OQG (Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented, 1).
Next steps
- See all 5 Novosource, Inc. clearances with predicates and recalls
- Run predicate analysis for product code JWH, Novosource, 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.