FDA.reportPublic FDA data

PONTiS Suture-Crimp Implant

Primary DI
00859210006117
Brand
PONTiS Suture-Crimp Implant
Company
PONTIS ORTHOPAEDICS, LLC
Model
400-3020
Catalog number
400-3020
Device description
PONTiS Dual Suture-Crimp Implant kit with Multifilament Stainless Steel Sutures and SS CrimpEach Kit contains:1x Dual #3-0 MFSS sutures with 2 straight needles1x SS Crimp collarSupplied pouched, sterilized with EO
Published
2017-09-12
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
GAQSuture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile
MBIFastener, Fixation, Nondegradable, Soft Tissue

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GAQSuture, Nonabsorbable, Steel, Monofilament And Multifilament, SterileGeneral, Plastic Surgery2
MBIFastener, Fixation, Nondegradable, Soft TissueOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00859210006117PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00859210006117008592100061178592100061170859210006117

GMDN Terms#

Term, Definition table
TermDefinition
Metallic suture, multifilamentA sterile, multiple-strand (multifilament), non-bioabsorbable wire made of metal (e.g., surgical steel, titanium) intended to join (approximate) the edges of a soft-tissue wound or incision by stitching (e.g., for abdominal wound closure, intestinal anastomosis, hernia repair), or transosseous (through bone) stitching (e.g., sternal closure); it may include an attached needle intended to be disposed of after single use. It is used primarily in orthopaedic, neurosurgical, and thoracic applications and provides temporary wound support until the wound sufficiently heals to withstand normal stress; it may be retained for permanent support. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
415-567-8935info@pontisorthopaedics.com

Regulatory Flags#

DUNS number
047775061
Device count
1
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00859210006001PONTiS Flexor Tendon Repair System400-3011400-30112016-09-01
00859210006032PONTiS Flexor Tendon Repair System401-3006401-30062016-09-01
00859210006070PONTiS Achilles Tendon Repair System600-4001600-40012016-09-01
00859210006018PONTiS Flexor Tendon Repair System400-3014400-30142016-09-01
08592110006100PONTiS Suture-Crimp Implant400-3019400-30192016-11-18
00859210006025PONTiS Flexor Tendon Repair System400-3031400-30312016-09-01
00859210006049PONTiS Flexor Tendon Repar System400-3015400-30152016-09-01

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