AFCALWMH0

GUDID 00841379158585

LAMINA HOOK, MEDIUM, ANGLED LEFT, EXTENDED

HYHTE HOLDINGS, INC.

Bone-screw internal spinal fixation system, non-sterile
Primary Device ID00841379158585
NIH Device Record Keye21e37f2-8bb7-4a0d-9c82-0a7812768ae9
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberAFCALWMH0
Catalog NumberAFCALWMH0
Company DUNS073029645
Company NameHYHTE HOLDINGS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100841379158585 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NKBThoracolumbosacral Pedicle Screw System

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


[00841379158585]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-09-10
Device Publish Date2018-08-09

Devices Manufactured by HYHTE HOLDINGS, INC.

00840085271861 - NA2025-03-06 EGPS, LUMBAR PEDICLE AWL
00840085271878 - NA2025-03-06 EGPS, LUMBAR PEDICLE PROBE, STRAIGHT
00840085271885 - NA2025-03-06 EGPS, LUMBAR PEDICLE PROBE, CURVED
00840085271892 - NA2025-03-06 EGPS, THORACIC PEDICLE PROBE, STRAIGHT
00840085271908 - NA2025-03-06 EGPS, THORACIC PEDICLE PROBE, CURVED
00840085271915 - NA2025-03-06 EGPS, REAMING PILOT DRILL, 3.5MM
00840085271922 - NA2025-03-06 EGPS, CORTICAL, TAP, 3.5MM
00840085271939 - NA2025-03-06 EGPS, CORTICAL, TAP, 4.0MM

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.