Atlas FDA

POLYESTER SPONGE PATTIE

FDA 510(k) clearance K862494 · decided 1986-07-30

Clearance details

K-number
K862494
Device name
POLYESTER SPONGE PATTIE
Applicant
American Silk Sutures, Inc.
Decision
Substantially Equivalent
Date received
1986-07-01
Decision date
1986-07-30
Days to decision
29 days
Clearance type
Traditional
Product code
HBA
Device class
2
Regulation number
882.4700
Medical specialty
Neurology
Advisory committee
Neurology
Location
Swampscott, MA, 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
Codman Surgical Patties & Strips (K193346)Integra LifeSciences Corporation2020-11-20
MEDLINE NEURO SPONGE (K140369)Medline Industries, Inc.2014-09-26
AMERICAN SURGICAL COMPANY/ NEUROSURGICAL SPONGES (BRAND) (K112598)American Surgical Company, LLC2013-06-20
DELICOT (K121822)American Surgical Company, LLC2012-09-10
NEUROSURGICAL SPONGES AND PADDLES AND NEURO PATTIES AND NEUROSPONGES (K073576)Harod Enterprises, Inc.2008-02-22
AESCULAP NEURO PATTIES (K062406)Aesculap, Inc.2006-09-15
AESCULAP NEURO PATTIES, NEUROSORB 4, 6, AND 75 (GREEN & WHITE) (K031008)Aesculap2003-05-09
TRAATEK COTTONOID PATTIES (K020736)Traatek, Inc.2002-06-03
NORAPAD PLAIN; NORAPAD TA (K014268)Perlei Medical, Inc.2002-03-27
PACIFIC SURGICAL PATTIES (K993019)V. Mueller Neuro/Spine2000-03-30
ULTRACELL NEURO SPONGES (K973083)Ultracell Medical Technologies, Inc.1997-12-09
AMERICAN SURGICAL SPONGES/NEUROSURGICAL SPONGES (K962807)American Surgical Sponges1997-05-02

Recalls involving this device

No recalls on record reference this clearance.