Black Belt Cervical Retractor Basic Set 7320-00

GUDID 00840199501762

Black Belt Cervical Retractor Basic Set, Consists of the Following: Black Finish Stainless Steel Frames and Blades. 1x 7320-22 - Korpectomy Retractor frame Right 1x 7320-20 - Retractor frame Left 1x 7320-30 - Retractor frame Offset 2x 7320-40 - Blade Inserting Clamps 2x 7322-34 - Pronged Blade 34mm, 2x 7322-40 - Pronged Blade 40mm, 2x 7322-45 - Pronged Blade 45mm, 2x 7322-50 - Pronged Blade 50mm, 2x 7322-55 - Pronged Blade 55mm, 2x 7322-60 - Pronged Blade 60mm, 2x 7322-70 - Pronged Blade 70mm, 2x 7324-34 - Blunt Blade 34mm, 2x 7324-40 - Blunt Blade 40mm, 2x 7324-45 - Blunt Blade 45mm, 2x 7324-50 - Blunt Blade 50mm, 2x 7324-55 - Blunt Blade 55mm, 2x 7324-60 - Blunt Blade 60mm, 2x 7324-70 - Blunt Blade 70mm, 4x 7326-40 - Two-Level Blade Pronged 40mm, 4x 7326-47 - Two-Level Blade Pronged 47mm, 4x 7326-55 - Two-Level Blade Pronged 55mm, 2x 7328-40 - Two-Level Blade Blunt 40mm, 2x 7328-47 - Two-Level Blade Blunt 47mm, 2x 7328-55 - Two-Level Blade Blunt 55mm, 1x 7320-90 - Sterilizing Instrument Case with silicone pads

KOROS U.S.A., INC.

Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable
Primary Device ID00840199501762
NIH Device Record Keyc6aadf06-823f-4d38-918c-0173f426a648
Commercial Distribution StatusIn Commercial Distribution
Brand NameBlack Belt Cervical Retractor Basic Set
Version Model Number7320-00
Catalog Number7320-00
Company DUNS007928633
Company NameKOROS U.S.A., INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com
Phone1-805-529-0825
Emailcustomerservice@korosUSA.com

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *Store in dry place at room temperature

Device Identifiers

Device Issuing AgencyDevice ID
GS100840199501762 [Direct Marking]
GS110840199501769 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GZTRetractor, Self-Retaining, For Neurosurgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


[00840199501762]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-07-06
Device Publish Date2021-06-28

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