FDA.reportPublic FDA data

N/A

Primary DI
00889024368804
Brand
N/A
Company
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.
Model
00-0923-002-00
Catalog number
00-0923-002-00
Device description
ZIMMER SPREADER BLOCK WIDTH: 2 INCHES
Published
2020-12-14
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
HSTApparatus, Traction, Non-Powered

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HSTApparatus, Traction, Non-PoweredOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00889024368804PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00889024368804008890243688048890243688040889024368804

GMDN Terms#

Term, Definition table
TermDefinition
Bed traction frameAn adjustable support structure usually attached to a patient's bed and designed for management of various orthopaedic conditions. It typically consists of a steel tubing structure that includes brackets and/or pulleys; it includes a post for the headboard and/or footboard, and often an adjustable-length top bar or rail with a hanging trapeze. The device is designed for use in combination with weights and/or other attachments to produce the desired traction in patients while permitting some freedom of motion. It is used to treat patients with fractures and other orthopaedic disorders (e.g., of the lower or cervical spine, hip).

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Width2Inch

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
1(800)348-2759zimmer.consumerrelations@zimmerbiomet.com

Regulatory Flags#

DUNS number
137354267
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
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
00889024616325Stablecut®XOXCEMTD3PKXOXCEMTD3PK2024-04-09
00889024616332Stablecut®XOXCMTLS3PKXOXCMTLS3PK2024-04-09
00889024647497Stablecut®11-353811-35382023-02-23
00889024647503Stablecut®11-353911-35392023-02-23
00889024647510Stablecut®11-354011-35402023-02-23
00889024647527Stablecut®11-354111-35412023-02-23
00889024647534Stablecut®11-354211-35422023-02-23
00889024647541Stablecut®11-354311-35432023-02-23
00889024647558Stablecut®11-360711-36072023-02-23
00889024647565Stablecut®11-360811-36082023-02-23
00889024647589Stablecut®11-377111-37712023-02-23
00889024647596Stablecut®5061095061092023-02-23
00889024647602Stablecut®5061115061112023-02-23
00889024647619Stablecut®5061425061422023-02-23
00889024647626Stablecut®5061405061402023-02-23
00889024647633Stablecut®5061415061412023-02-23
00889024647640Stablecut® Vanguard™32-70036932-7003692023-02-23
00880304537880Stablecut®5061135061132022-10-03
00880304542464Stablecut®5061145061142022-10-03
00889024493254Stablecut®10070100CR110-0701-00C-R12019-02-22

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00615521004712ArthrexALLEN MEDICAL SYSTEMS, INC.HST2024-05-23
00615521004736ArthrexALLEN MEDICAL SYSTEMS, INC.HST2024-05-23
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00615521004828ArthrexALLEN MEDICAL SYSTEMS, INC.HST2024-05-23
00615521004842ArthrexALLEN MEDICAL SYSTEMS, INC.HST2024-05-23
00840277130495Innomed, Inc.INNOMED, INC.HST2024-05-09
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00615521001490ALLENALLEN MEDICAL SYSTEMS, INC.HST2023-07-31
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00615521012823ALLENALLEN MEDICAL SYSTEMS, INC.HST2023-07-31
00615521021160ALLENALLEN MEDICAL SYSTEMS, INC.HST2023-07-31
00615521021177ALLENALLEN MEDICAL SYSTEMS, INC.HST2023-07-31
00615521021184ALLENALLEN MEDICAL SYSTEMS, INC.HST2023-07-31
10845854082959ParadigmConmed CorporationHST2023-06-23