FDA.reportPublic FDA data

OvertureTi

Primary DI
00810129550146
Brand
OvertureTi
Company
Overture Resurfacing Inc
Model
PKG-90-OVR-200017
Published
2023-10-18
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

Product Codes#

Code, Name table
CodeName
HSXProsthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HSXProsthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/PolymerOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K221292000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K221292000Uni Knee Resurfacing SystemOverture Resurfacing, Inc.2023-03-10HSX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810129550146PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810129550146008101295501468101295501460810129550146

GMDN Terms#

Term, Definition table
TermDefinition
Unicondylar knee prosthesisA sterile artificial substitute for the bearing surface of only one femoral condyle and corresponding tibial condyle of the knee (medial or lateral condyle) implanted during primary or revision knee replacement. It typically consists of femoral and tibial components and a knee insert which are made of metal or polyethylene (PE); fixation devices for implantation (e.g., screws) may be included and implantation may be performed with or without bone cement. The device is indicated in unicompartmental disease and/or damage (e.g., from arthritis) to the bearing surfaces of the knee.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Width0

Regulatory Flags#

DUNS number
119105665
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
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810129551846OvertureTi90-S01-1022502025-07-23
00810129551723OvertureTiPKG-90-OSP-1017302025-03-14
00810129551730OvertureTiPKG-90-OSP-1020352025-03-14
00810129551747OvertureTiPKG-90-OSP-1022402025-03-14
00810129551754OvertureTiPKG-90-OSP-2000172025-03-14
00810129551761OvertureTiPKG-90-OSP-2000222025-03-14
00810129551778OvertureTiPKG-90-OSP-2000252025-03-14
00810129551785OvertureTiPKG-90-OSP-3600172025-03-14
00810129551792OvertureTiPKG-90-OSP-3600202025-03-14
00810129551808OvertureTiPKG-90-OSP-3600222025-03-14
00810129551815OvertureTiPKG-90-OSP-4000002025-03-14
00810129550221OvertureTiPKG-90-OVR-3500172024-12-06
00810129550238OvertureTiPKG-90-OVR-3500202024-12-06
00810129550245OvertureTiPKG-90-OVR-3500222024-12-06
00810129550276OvertureTi90-OVR-5000172023-10-25
00810129550290OvertureTi90-OVR-5000222023-10-25
00810129550306OvertureTi90-OVR-5000252023-10-25
00810129550337OvertureTi90-OVR-5017302023-10-25
00810129550375OvertureTi90-OVR-5020352023-10-25
00810129550412OvertureTi90-OVR-5022402023-10-25

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
05404028001257SurgiCase PlannerMaterialise NVHSX2026-05-28
05404028000922SurgiCase PlannerMaterialise NVHSX2025-05-14
00822409130153N/AOrtho Development CorporationHSX2025-03-17
00822409130160N/AOrtho Development CorporationHSX2025-03-17
00822409130177N/AOrtho Development CorporationHSX2025-03-17
00822409130184N/AOrtho Development CorporationHSX2025-03-17
00822409130191N/AOrtho Development CorporationHSX2025-03-17
00822409130207N/AOrtho Development CorporationHSX2025-03-17
00822409130214N/AOrtho Development CorporationHSX2025-03-17
00822409130221N/AOrtho Development CorporationHSX2025-03-17
00822409130238N/AOrtho Development CorporationHSX2025-03-17
00822409130245N/AOrtho Development CorporationHSX2025-03-17
00822409130252N/AOrtho Development CorporationHSX2025-03-17
00822409130269N/AOrtho Development CorporationHSX2025-03-17
00810129550221OvertureTiOverture Resurfacing IncHSX2024-12-06
00810129550238OvertureTiOverture Resurfacing IncHSX2024-12-06
00810129550245OvertureTiOverture Resurfacing IncHSX2024-12-06
00810129550016OvertureTiOverture Resurfacing IncHSX2023-10-18
00810129550054OvertureTiOverture Resurfacing IncHSX2023-10-18
00810129550092OvertureTiOverture Resurfacing IncHSX2023-10-18
00810129550160OvertureTiOverture Resurfacing IncHSX2023-10-18
00810129550177OvertureTiOverture Resurfacing IncHSX2023-10-18
00810129550191OvertureTiOverture Resurfacing IncHSX2023-10-18
00810129550207OvertureTiOverture Resurfacing IncHSX2023-10-18
00810129550214OvertureTiOverture Resurfacing IncHSX2023-10-18
00885556779989VISIONAIRESmith & Nephew, Inc.HSX2021-09-22
00885556780039VISIONAIRESmith & Nephew, Inc.HSX2021-09-22
E314SURGICASEKNEEPLAN0SurgiCase PlannerMaterialise NVHSX2018-10-17
07613327127423INSTRUMENTHowmedica Osteonics Corp.HSX2017-11-24
07613327127447INSTRUMENTHowmedica Osteonics Corp.HSX2017-11-24