Distraction Screw Caspar type 800-500

GUDID 00810607000248

Distraction Screw Caspar type

ACRA-CUT INC

Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use
Primary Device ID00810607000248
NIH Device Record Key79530354-a3ee-4d6a-9ecd-e8a9a480b6b0
Commercial Distribution StatusIn Commercial Distribution
Brand NameDistraction Screw Caspar type
Version Model Number800-500
Catalog Number800-500
Company DUNS612611459
Company NameACRA-CUT INC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone9782632210
Emailinfo@acracut.com
Phone9782632210
Emailinfo@acracut.com
Phone9782632210
Emailinfo@acracut.com
Phone9782632210
Emailinfo@acracut.com
Phone9782632210
Emailinfo@acracut.com
Phone9782632210
Emailinfo@acracut.com
Phone9782632210
Emailinfo@acracut.com
Phone9782632210
Emailinfo@acracut.com
Phone9782632210
Emailinfo@acracut.com
Phone9782632210
Emailinfo@acracut.com
Phone9782632210
Emailinfo@acracut.com
Phone9782632210
Emailinfo@acracut.com
Phone9782632210
Emailinfo@acracut.com
Phone9782632210
Emailinfo@acracut.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100810607000248 [Primary]

FDA Product Code

KDCInstrument, Surgical, Disposable

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[00810607000248]

Radiation Sterilization

[00810607000248]

Radiation Sterilization

[00810607000248]

Radiation Sterilization

[00810607000248]

Radiation Sterilization

[00810607000248]

Radiation Sterilization

[00810607000248]

Radiation Sterilization

[00810607000248]

Radiation Sterilization

[00810607000248]

Radiation Sterilization

[00810607000248]

Radiation Sterilization

[00810607000248]

Radiation Sterilization

[00810607000248]

Radiation Sterilization

[00810607000248]

Radiation Sterilization

[00810607000248]

Radiation Sterilization

[00810607000248]

Radiation Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-05-01

Devices Manufactured by ACRA-CUT INC

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00810607002211 - ACRA-CUT2018-11-22 Disposable Cranial Perforator
00810607002310 - ACRA-CUT2018-11-22 Disposable Cranial Perforator
00810607002419 - ACRA-CUT2018-11-22 Disposable Cranial Perforator
00810607002433 - ACRA-CUT2018-11-22 Disposable Cranial Perforator
00810607002518 - ACRA-CUT2018-11-22 Disposable Cranial Perforators
00810607002532 - ACRA-CUT2018-11-22 Disposable Cranial Perforator
00810607002556 - ACRA-CUT2018-11-22 Disposable Cranial Perforator
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