FDA.reportPublic FDA data

NA

Primary DI
23596010495918
Brand
NA
Company
Smith & Nephew, Inc.
Model
7210149
Catalog number
7210149
Device description
BONE TUNNEL PLUGS CANN 7-12MM LTX
Published
2015-08-30
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HRXARTHROSCOPE

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HRXArthroscopeOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K925437000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K925437000ACUFEX CANNULATED BONE TUNNEL PLUGSCufex Microsurgical, Inc.1992-12-24HRX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
23596010495918PackageGS16In Commercial Distribution
03596010495914PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
2359601049591823596010495918
03596010495914035960104959143596010495914

GMDN Terms#

Term, Definition table
TermDefinition
Bone tunnel plug, cannulatedA sterile device intended to be inserted into a bone tunnel during an arthroscopic procedure to reduce the loss of the irrigation fluid used to maintain visualization, while allowing the passage of instruments (e.g., probes, guide pins, shavers and graspers) through its lumen to access the joint. It is a short, rigid, cannulated tube which tapers distally with a penetrable seal on the proximal end. It is inserted manually into the bone tunnel, or may be supplied with dedicated instruments for insertion (e.g., obturator). The device is available in a variety of diameters, and is typically made of plastic. This is a single-use device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify000

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)238-7538GUDID@SMITH-NEPHEW.COM

Regulatory Flags#

DUNS number
045483575
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
true
No natural rubber latex
false
Sterilization required before use
false

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00885556833964Salto Talaris Total Ankle ProsthesisMJV220TMJV220T2022-12-22
00885556833971Salto Talaris Total Ankle ProsthesisMJV221TMJV221T2022-12-22
00885556833988Salto Talaris Total Ankle ProsthesisMJV229TMJV229T2022-12-22
00885556834237Silicone Toe SystemCGT-205TCGT-205T2022-12-22
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00885556835029Ti6 Internal Fixation SystemDS1007DS10072022-12-22
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00885556837856Total Foot System 2220425022042502022-12-22
00885556838785Total Foot System 2282302728230272022-12-21
00885556841631XT Revision Ankle Replacement SystemMJU984TMJU984T2022-12-21
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