PuraSinus
FDA 510(k) clearance K183015 · decided 2019-04-12
Clearance details
- K-number
- K183015
- Device name
- PuraSinus
- Applicant
- 3-D Matrix, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2018-10-31
- Decision date
- 2019-04-12
- Days to decision
- 163 days
- Clearance type
- Traditional
- Product code
- NHB
- Device class
- 2
- Regulation number
- 874.3620
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- Location
- Needham, MA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch 3-D Matrix
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| SeptAlign (SPLN001) (K260620) | Spirair, Inc. | 2026-07-30 |
| SeptAlign (K251790) | Spirair, Inc. | 2026-01-16 |
| SeptAlign (K233569) | Spirair, Inc. | 2024-03-22 |
| Spirair Nasal Septal Strap (K223167) | Spirair, Inc. | 2023-08-17 |
| PosiSep EAR Fragmentable Ear Dressing (K210411) | Hemostasis, LLC | 2022-05-05 |
| LATERA Absorbable Nasal Implant System (K192661) | Entellus Medical, Inc. (Aka Stryker Ent) | 2019-11-10 |
| Latera Absorbable Nasal Implant (K161191) | Spirox, Inc. | 2016-06-23 |
| INEX Absorbable Nasal Implant (K152958) | Spirox, Inc. | 2015-12-04 |
| SPIROX INEX DEVICE (K132920) | Spirox, Inc. | 2014-06-10 |
| MEROGEL INJECTABLE BIORESORBABLE NASAL DRESSING AND SINUS STENT AND OTOLOGIC GEL (K122434) | Medtronic Xomed | 2012-10-31 |
| PDS PLATES (K092590) | ETHICON, Inc. | 2010-02-17 |
| NASOPORE EAR (K070715) | Polyganics B.V., | 2007-05-07 |
Recalls involving this device
No recalls on record reference this clearance.