Atlas FDA

ACUITY STEERABLE STYLET ACCESSORY

FDA 510(k) clearance K053019 · decided 2006-03-03

Clearance details

K-number
K053019
Device name
ACUITY STEERABLE STYLET ACCESSORY
Applicant
Guidant Corporation
Decision
Substantially Equivalent
Date received
2005-10-26
Decision date
2006-03-03
Days to decision
128 days
Clearance type
Traditional
Product code
DRB
Device class
2
Regulation number
870.1380
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
St Paul, MN, 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
Arrow Stiffening Stylet (K220280)Arrow International, LLC (A subsidiary of Teleflex, Inc.)2022-08-30
Biotronik Stylets (K191469)Biotronik, Inc.2019-08-01
GaltTWS (K182660)Galt Medical Corp.2019-05-30
Liberator Beacon Tip Locking Stylet (K170298)Cook Incorporated2017-10-18
LLD EZ (K142116)Spectranetics, Inc.2014-08-12
STYLET, MODELS 4060, 4062, 4064, 4090, 4091 AND 4078 (K090163)St Jude Medical2009-04-01
MOND RVOT STYLET MODELS 4140, 4141, 4150, 4151 (K080924)St. Jude Medical, Cardiac Rhythm Management Divisi2008-04-30
ST. JUDE MEDICAL, CPS DUO LEFT HEART LEAD DELIVERY SYSTEM (K072864)St. Jude Medical, Cardiac Rhythm Management Divisi2008-03-13
EASYTRAK 2 STYLET, MODELS 4826, 4829, 4832. (K052965)Guidant Corporation2006-02-13
SPECTRANETICS LLD CS, MODEL 518-039 (K043401)Spectranetics Corp.2005-03-16
STEERABLE STYLET (K040001)Synovis Surgical Innovations2004-03-09
MEDTRONIC STYLET KIT, MODELS 6282, 6293, AND 6254 (K010906)Medtronic Vascular2001-04-05

Recalls involving this device

No recalls on record reference this clearance.