Atlas FDA

INEX Absorbable Nasal Implant

FDA 510(k) clearance K152958 · decided 2015-12-04

Clearance details

K-number
K152958
Device name
INEX Absorbable Nasal Implant
Applicant
Spirox, Inc.
Decision
Substantially Equivalent
Date received
2015-10-07
Decision date
2015-12-04
Days to decision
58 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
Menlo Park, CA, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Spirox

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.

RecordFirmDate
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, LLC2022-05-05
LATERA Absorbable Nasal Implant System (K192661)Entellus Medical, Inc. (Aka Stryker Ent)2019-11-10
PuraSinus (K183015)3-D Matrix, Inc.2019-04-12
Latera Absorbable Nasal Implant (K161191)Spirox, Inc.2016-06-23
SPIROX INEX DEVICE (K132920)Spirox, Inc.2014-06-10
MEROGEL INJECTABLE BIORESORBABLE NASAL DRESSING AND SINUS STENT AND OTOLOGIC GEL (K122434)Medtronic Xomed2012-10-31
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.