Citrepore
FDA 510(k) K240450 · Acuitive Technologies, Inc.
510(k) numberK240450
Submission
- Device name
- Citrepore
- Applicant
- Acuitive Technologies, Inc.
Alendale, NJ, US - Received
- February 15, 2024
- Decision date
- November 6, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MQV – Filler, Bone Void, Calcium Compound
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3045
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code MQV
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262230 | Mg OSTEOREVIVE;Mg OSTEOCRETEMQV · Traditional | Bone Solutions, Inc. | 09/11/2026SE |
| K260364 | Device 300419 StripMQV · Traditional | Geistlich Pharma AG | 06/02/2026SE |
| K252797 | JAZBI Resorbable Bone Void FillerMQV · Traditional | Sdip Innovations Pty, Ltd. | 05/26/2026SE |
| K261008 | Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive…MQV · Special | Stryker Spine | 04/24/2026SE |
| K253524 | Adaptos®Fuse Bone GraftMQV · Traditional | Biomendex OY | 02/17/2026SE |
| K253147 | FIBERGRAFT BG Putty GPS Bone Graft Substitute FIBERGRAFT BG Putty Bone Graft…MQV · Special | Prosidyan, Inc. | 10/22/2025SE |
| K251522 | Mg OSTEOINJECT; Mg OSTEOREVIVE; Mg OSTEOCRETEMQV · Traditional | Bone Solutions, Inc. | 10/13/2025SE |
| K252085 | Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom)MQV · Traditional | Wright Medical Technology, Inc. (Stryker… | 09/30/2025SE |
| K251556 | Device 300423 GranulesMQV · Traditional | Geistlich Pharma AG | 07/17/2025SE |
| K251720 | OsteoFlo HydroFiberMQV · Special | SurGenTec, LLC | 07/02/2025SE |
More from SurGenTec, LLC
| 510(k) | Device | Decision |
|---|---|---|
| K232592 | Citrelock® DuoMBI · Special | 09/20/2023SE |
| K221468 | Citregen Tendon Interference Screw (TIS), Citrelock Tendon Fixation Device…MAI · Traditional | 02/14/2023SE |
| K220833 | Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and Citrelock…MAI · Traditional | 11/04/2022SE |
| K210239 | CITRESPLINE and CITRELOCK ACL ImplantsMAI · Special | 02/24/2021SE |
| K203334 | The Citrefix Knotless Suture AnchorMAI · Traditional | 02/05/2021SE |
| K200725 | Citregen Tendon Interference Screw and CitrelockMAI · Traditional | 10/07/2020SE |
Questions and answers
When was Citrepore cleared by the FDA?
Citrepore (K240450) received a 510(k) decision of Substantially Equivalent on November 6, 2024, 265 days after the submission was received.
What is the product code of K240450?
The FDA product code is MQV – Filler, Bone Void, Calcium Compound, a Class II (moderate risk) device regulated under 21 CFR 888.3045.