Renu Gel
FDA 510(k) K150400 · Cytophil, Inc.
510(k) numberK150400
Submission
- Device name
- Renu Gel
- Applicant
- Cytophil, Inc.
East Troy, WI, US - Received
- February 18, 2015
- Decision date
- April 6, 2015
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MIX – System, Vocal Cord Medialization
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 874.3620
- Specialty
- Ear, Nose, Throat
- Implant
- Yes
Other 510(k)s with product code MIX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K240919 | Silk Voice (SMI-04)MIX · Special | Sofregen Medical | 05/03/2024SE |
| K180631 | Silk VoiceMIX · Traditional | Sofregen Medical, Inc. | 11/08/2018SE |
| K121795 | Calcium Hydroxylapatite Vocal Fold ImplantMIX · Traditional | Cytophil, Inc. | 02/22/2013SE |
| K083783 | VF LiquigelMIX · Traditional | Coapt Systems, Inc. | 09/11/2009SE |
| K081816 | Vocalis and Vocalis SMMIX · Traditional | Cytophil, Inc. | 01/05/2009SE |
| K081815 | Vocalis GelMIX · Traditional | Cytophil, Inc. | 01/05/2009SE |
| K080956 | Modification to VF Gel PlusMIX · Special | Coapt Systems, Inc. | 04/25/2008SE |
| K071663 | VF Gel PlusMIX · Traditional | Coapt Systems, Inc. | 02/15/2008SE |
| K070090 | Radiesse Laryngeal ImplantMIX · Special | Bioform Medical, Inc. | 03/01/2007SE |
| K060815 | Juliesse Injectable Laryngeal Augmentation ImplantMIX · Special | Bioform Medical, Inc. | 04/18/2006SE |
More from Bioform Medical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K121795 | Calcium Hydroxylapatite Vocal Fold ImplantMIX · Traditional | 02/22/2013SE |
| K102937 | Osteophil Beta-TcpMQV · Traditional | 12/27/2010SE |
| K093871 | Periophil B-TcpLYC · Traditional | 04/22/2010SE |
| K092788 | Periophil BiphasicLYC · Traditional | 12/18/2009SE |
| K081816 | Vocalis and Vocalis SMMIX · Traditional | 01/05/2009SE |
| K081815 | Vocalis GelMIX · Traditional | 01/05/2009SE |
| K072219 | Cytophil Tissue MarkerNEU · Traditional | 01/18/2008SE |
Questions and answers
When was Renu Gel cleared by the FDA?
Renu Gel (K150400) received a 510(k) decision of Substantially Equivalent on April 6, 2015, 47 days after the submission was received.
What is the product code of K150400?
The FDA product code is MIX – System, Vocal Cord Medialization, a Class II (moderate risk) device regulated under 21 CFR 874.3620.