FDA.reportPublic FDA data

BC Reflex Uni

Primary DI
00688346001341
Brand
BC Reflex Uni
Company
Laboratoires Bodycad Inc
Model
018-001
Catalog number
018-001
Published
2021-12-13
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
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
K212307000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K212307000BC Reflex Uni Knee SystemBodycad Laboratories, Inc.2021-10-12HSX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00688346001341PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00688346001341006883460013416883460013410688346001341

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.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
202981171
Device count
1
Serial number
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00688346002485Fine osteotomy HA 4.5 Cortical Bone Screw - L30mm037-106-0302023-10-20
00688346002492Fine osteotomy HA 4.5 Cortical Bone Screw - L32mm037-106-0322023-10-20
00688346002508Fine osteotomy HA 4.5 Cortical Bone Screw - L34mm037-106-0342023-10-20
00688346002515Fine osteotomy HA 4.5 Cortical Bone Screw - L36mm037-106-0362023-10-20
00688346002522Fine osteotomy HA 4.5 Cortical Bone Screw - L38mm037-106-0382023-10-20
00688346002539Fine osteotomy HA 4.5 Cortical Bone Screw - L40mm037-106-0402023-10-20
00688346002546Fine osteotomy HA 4.5 Cortical Bone Screw - L42mm037-106-0422023-10-20
00688346002553Fine osteotomy HA 4.5 Cortical Bone Screw - L44mm037-106-0442023-10-20
00688346002560Fine osteotomy HA 4.5 Cortical Bone Screw - L46mm037-106-0462023-10-20
00688346002577Fine osteotomy HA 4.5 Cortical Bone Screw - L48mm037-106-0482023-10-20
00688346002584Fine osteotomy HA 4.5 Cortical Bone Screw - L50mm037-106-0502023-10-20
00688346002591Fine osteotomy HA 4.5 Cortical Bone Screw - L52mm037-106-0522023-10-20
00688346002607Fine osteotomy HA 4.5 Cortical Bone Screw - L54mm037-106-0542023-10-20
00688346002614Fine osteotomy HA 4.5 Cortical Bone Screw - L56mm037-106-0562023-10-20
00688346002621Fine osteotomy HA 4.5 Cortical Bone Screw - L58mm037-106-0582023-10-20
00688346002638Fine osteotomy HA 4.5 Cortical Bone Screw - L60mm037-106-0602023-10-20
00688346002645Fine osteotomy HA 4.5 Cortical Bone Screw - L62mm037-106-0622023-10-20
00688346002652Fine osteotomy HA 4.5 Cortical Bone Screw - L64mm037-106-0642023-10-20
00688346002669Fine osteotomy HA 4.5 Cortical Bone Screw - L66mm037-106-0662023-10-20
00688346002676Fine osteotomy HA 4.5 Cortical Bone Screw - L68mm037-106-0682023-10-20

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Primary DI, Brand, Company table
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