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Product codes
NLL
Product code NLL
Device name
Staple, Implantable, Reprocessed
Medical specialty
General, Plastic Surgery
Device class
2
Regulation number
878.4750
Review panel
SU
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
N
Summary malfunction reporting
Ineligible
Definition
Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).
Source
FDA openFDA device classification dataset
Related 510(k) Records
#
510(k), Device, Applicant table
510(k)
Device
Applicant
Decision date
K070930
REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERS
Sterilmed, Inc.
2007-10-18
K070859
REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERS
Sterilmed, Inc.
2007-09-12
K033578
REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERS
Clearmedical, Inc.
2005-07-11