Duns Number:482661753
Device Description: PEEK Anchor with (1) 2.5mm Blue PERMATAPE Braided Flat Suture, 38 inches (96 cm) and (1) W PEEK Anchor with (1) 2.5mm Blue PERMATAPE Braided Flat Suture, 38 inches (96 cm) and (1) White/Black, Size 2 (5 metric) PERMACORD Braided Suture, 36 inches (91cm), (1) Utility Shuttle Suture
Catalog Number
222363
Brand Name
HEALIX ADVANCE PEEK ANCHOR w/PERMATAPE PERMACORD
Version/Model Number
222363
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K170639
Product Code
MBI
Product Code Name
Fastener, fixation, nondegradable, soft tissue
Public Device Record Key
528c23e2-c6f7-428d-bcf2-f24aa026da29
Public Version Date
March 21, 2019
Public Version Number
6
DI Record Publish Date
October 27, 2017
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 972 |
2 | A medical device with a moderate to high risk that requires special controls. | 6382 |
3 | A medical device with high risk that requires premarket approval | 20 |
U | Unclassified | 20 |