AccessGUDID - DEVICE: Nano fx® (M528FURS11010)

GUDID

Device Identifier (DI) Information

Brand Name: Nano fx®
Version or Model: FURS-1101
Commercial Distribution Status: In Commercial Distribution
Catalog Number: FURS-1101
Company Name: ARTHROSURFACE INCORPORATED

Primary DI Number: M528FURS11010
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 144666109 *Terms of Use

Device Description: Pleuristik, NanoFracture, Hip

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
61411	Subchondral bone needling device	A sterile, metallic surgical instrument intended to be used to create thin channels in the bone layer beneath articular cartilage to enable migration of bone marrow (blood stem) cells to promote healing of a cartilage defect. Otherwise known as nanofracture, subchondral bone needling uses non-rotational force (hammering) during an arthroscopic procedure. It is made of metal [e.g., nickel-titanium alloy (Nitinol)] in the form of a long thin spike with a bulbous proximal end and is typically used with a reusable handle (not included). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LXH	Orthopedic Manual Surgical Instrument

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 349f5e0f-a199-4a37-a7d0-2aa369a04d50
Public Version Date: March 29, 2018
Public Version Number: 2
DI Record Publish Date: July 31, 2016

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: Yes
Manufacturing Date: Yes
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: 508-520-3003
Email: CONTACT@ARTHROSURFACE.COM

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