Atlas FDA

SPINAL NEEDLE

FDA 510(k) clearance K960405 · decided 1996-02-28

Clearance details

K-number
K960405
Device name
SPINAL NEEDLE
Applicant
Promex, Inc.
Decision
Substantially Equivalent
Date received
1996-01-29
Decision date
1996-02-28
Days to decision
30 days
Clearance type
Traditional
Product code
MIA
Device class
2
Regulation number
868.5150
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Indianapolis, IN, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Portex® Lancet Point Spinal Needles with NRFit™ connectors, Portex® Pencil Point Spinal Needles with NRFit™ connectors (K172800)Smiths Medical Asd, Inc.2018-06-14
FLEXIBLE INTRODUCER CANNULA, MODEL 135-1837 (K051860)Epimed International, Inc.2005-08-22
SPINAL ANESTHESIA NEEDLES AND INTRODUCER NEEDLES (K983858)Sims Portex, Inc.1999-01-29
CLEAR HUB SPINAL NEEDLE 14GA, 16GA, 17GA, 18GA, 20GA, 21GA, 22GA, 25GA, 26GA AND 27GA (K982269)Allegiance Healthcare Corp.1998-07-23
REGANES SPINAL NEEDLE (VARIOUS) (K971645)Avid N.I.T., Inc.1997-08-01
NEO-CARE LUMBER PUNCTURE KIT (K970997)Klein-Baker Medical, Inc.1997-05-22
GLOBAL MEDICAL PRODUCTS SPINAL,CONICAL TIP (SPROTTLE STYLE), WHITACRE STYLE NEEDLES (K961324)Global Medical Prods, Inc.1996-07-02
ACUFEX T-FIX DELIVERY SYSTEM (K942442)Acufex Microsurgical, Inc.1994-12-05
SPINAL CORD ACCESS EPIDURAL INTRODUCER SYSTEM (K904380)Custom Medical Concepts, Inc.1993-04-08

Recalls involving this device

No recalls on record reference this clearance.