Allograft Delivery Device (OFAC-C)
FDA 510(k) K233368 · Bioventus, LLC
510(k) numberK233368
Submission
- Device name
- Allograft Delivery Device (OFAC-C)
- Applicant
- Bioventus, LLC
Durham, NC, US - Received
- October 2, 2023
- Decision date
- June 25, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FMF – Syringe, Piston
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5860
- Specialty
- General Hospital
Other 510(k)s with product code FMF
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262581 | GraftGun Universal Graft Delivery System (GDS®)FMF · Special | SurGenTec, LLC | 08/26/2026SE |
| K252184 | SOL-M Luer Lock Syringe with Exchangeable Needle TrayFMF · Traditional | Sol-Millennium Medical, Inc. | 08/25/2026SE |
| K253747 | Disposable Pen Injector (KXYC-03C02, KXYC-03A03)FMF · Traditional | Jiangsu Enjosim Medical Technology Co., Ltd. | 08/14/2026SE |
| K260208 | Ultra-Fine SAFETY Insulin SyringeFMF · Traditional | embecta Medical II, LLC | 07/13/2026SE |
| K253110 | Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeFMF · Traditional | Sol-Millennium Medical, Inc. | 06/18/2026SE |
| K260514 | Profoject Safety Needle; Profoject Syringe with Safety Needle; Profoject Low Dead…FMF · Traditional | CMT Health PTE., Ltd. | 06/12/2026SE |
| K253112 | Sofjec (Single use Needle); Sofjec (Single use Syringe with or without Needle); Sofjec…FMF · Special | Hlb Lifescience Co., Ltd. | 05/21/2026SE |
| K252279 | Sterile Hypodermic Syringe for Single Use (20ml, 30ml, 50ml, 60ml)FMF · Traditional | Chirana T.Injecta,A.S. | 04/17/2026SE |
| K253068 | Profoject Insulin Syringes; Profoject Safelock Disposable Insulin SyringeFMF · Traditional | CMT Health PTE., Ltd. | 02/23/2026SE |
| K253769 | Instylla Delivery KitFMF · Special | Instylla, Inc. | 12/22/2025SE |
More from Instylla, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K253877 | StimTrial Neuromodulation SystemGZF · Special | 08/26/2026SE |
| K243782 | StimTrial Neuromodulation SystemGZF · Traditional | 07/16/2025SE |
| K243678 | TalisMann Neuromodulation SystemGZF · Traditional | 07/03/2025SE |
| K233490 | SIGNAFUSE Bioactive Strip (SBS); SIGNAFUSE PuttyMQV · Traditional | 12/05/2023SE |
| K193513 | SIGNAFUSE Bioactive Bone GraftMQV · Traditional | 06/18/2020SE |
| K162860 | MCS Bone GraftMQV · Traditional | 02/13/2017SE |
Questions and answers
When was Allograft Delivery Device (OFAC-C) cleared by the FDA?
Allograft Delivery Device (OFAC-C) (K233368) received a 510(k) decision of Substantially Equivalent on June 25, 2024, 267 days after the submission was received.
What is the product code of K233368?
The FDA product code is FMF – Syringe, Piston, a Class II (moderate risk) device regulated under 21 CFR 880.5860.