SHOULDER: Acromio-clavicular; Bankart repair; Biceps tenodesis; Capsule shift/capsulolabral reconstruction; Deltoid repair; Rotator cuff repair; SLAP lesion repair. ANKLE: Achilles tendon repair/reconstruction; Lateral instability; Medial instability; Midfoot reconstructions. FOOT: Hallux valgus reconstruction. WRIST: Scapholunate ligament reconstruction. HAND: Ulnar or lateral collateral ligament reconstruction. ELBOW: Biceps tendon reattachment; Tennis elbow repair. KNEE: Extra capsular reconstruction, ITB tenodesis; Lateral ligament; Patellar ligament and tendon avulsion repairs; Posterior oblique ligament or joint capsule to tibia; Joint capsule closure to anterior proximal tibia; Medial collateral ligament. BNS: Fixation in pubic bone for bladder neck suspension using USP #2 Class I nonabsorbable synthetic suture (e.g. polypropylene). A minimum of 2 Anchors should be used in this procedure.

Device Description

The only proposition of this 510(k) submission is to add a "MR-Conditional" statement and symbol to all applicable product package-insert and labels of GII™ Anchor devices. Technological characteristics including indications, product design, material, and packaging are the same as the predicate devices.

AI/ML Overview

The provided text describes a 510(k) submission for the DePuy Mitek GII™ Anchor, focusing on adding an "MR-Conditional" statement and symbol to the product. This submission is for a modification to an already marketed device, not for a new medical device that performs a diagnostic or predictive function.

Therefore, the document does not contain the information requested in the prompt regarding acceptance criteria, device performance metrics (like sensitivity, specificity, AUC), sample sizes for test/training sets, expert qualifications, or adjudication methods typically associated with studies proving the performance of AI/analytic devices.

The "Nonclinical Testing" section mentions "MRI Testing using a scanner operating with a static magnetic field was performed on the DePuy Mitek metal implant devices." and "Results of 'Evaluation of Magnetic Field Interactions, Heating, and Artifacts' have demonstrated that the currently marketed DePuy Mitek GII™ Anchors are 'MR-conditional'." This refers to physical testing to ensure safety in an MRI environment, not a study evaluating an algorithm's performance.

Summary

{0}------------------------------------------------

Image /page/0/Picture/1 description: The image shows the DePuy Mitek Inc. logo with the tagline "never stop moving." The logo is black and white and features the DePuy name in a stylized font. Below the name is the text "Mitek Inc." and ".johnson&johnson company" in a smaller font. The tagline is in a cursive font and is located to the right of the logo.

GII™ ANCHOR PRODUCT: SUBMISSION DATE: AUGUST 22°0, 2011 SUBMISSION TYPE: TRADITIONAL

JAN 1 3 2012

ATTACHMENT 1

5 10(k) SUMMARY - DePuy Mitek GII™ ANCHOR

SUBMITTER'S NAME AND ADDRESS

DePuy Mitek, Inc. a Johnson & Johnson company 325 Paramount Drive Raynham, MA 02767

CONTACT PERSON

Deep Pal Senior Regulatory Affairs Specialist DePuy Mitek, Inc. a Johnson & Johnson company 325 Paramount Drive Raynham, MA 02767

TELEPHONE	508-828-3339
FACSIMILE	508-977-6911
E-MAIL	dpal3@its.jnj.com
DATE PREPARED	August 22nd, 2011

NAME OF MEDICAL DEVICE

with the state of the country and control control of the contrôlection of the contrôlean con-COMMON NAME
Bone Anchors, Screws

TRADE NAME/PROPRIETARY NAME

GII™ Anchor .

SUBSTANTIAL EQUIVALENCE

There are no changes being made to the indications, product designs, material, packaging, and to the manufacturing processes. The only proposition of this 510(k) submission is to add a generic "MR-Conditional" statement and symbol to the product package insert and labels.

GI™ Anchor . K915888
Various Metal Implants K11631 .

DEVICE CLASSIFICATION

•	GII™ Anchor - K915889
o	Device Classification:	II
o	Device Classification Name:	Fastener, Fixation, Nondegradable, Soft tissueStaple, Fixation, Bone
o	Regulation Number:	888.3040-Smooth or threaded metallic bone fixation fastener888.3030-Single/multiple component metallic bone fixationappliances and accessories
o	Classification Product Code:	MBI, JDR

{1}------------------------------------------------

Image /page/1/Picture/1 description: The image shows the DePuy Synthes logo. The logo includes the text "DePuy Mitek Inc. a Johnson-Johnson company" and the tagline "never stop moving". The logo is black and white and is positioned in the upper left corner of the image.

GII™ ANCHOR PRODUCT: SUBMISSION DATE: AUGUST 2200, 2011 SUBMISSION TYPE: TRADITIONAL

ATTACHMENT 1

1 : 1 / 1 /

Continues ...

5 I 0(k) SUMMARY - DePuy Mitek MRI STATEMENT FOR METAL IMPLANTS

INDICATIONS FOR USE

GII Anchors SHOULDER: Acromio-clavicular; Bankart repair; Biceps tenodesis; Capsule shift/capsulolabral reconstruction; Deltoid repair; Rotator cuff repair; SLAP lesion repair. ANKLE: Achilles tendon repair/reconstruction; Lateral instability; Medial instability; Midfoot reconstructions.

FOOT: Hallux valgus reconstruction.

WRIST: Scapholunate ligament reconstruction.

HAND: Ulnar or lateral collateral ligament reconstruction.

ELBOW: Biceps tendon reattachment; Tennis elbow repair.

KNEE: Extra capsular reconstruction, ITB tenodesis; Lateral ligament; Patellar ligament and tendon avulsion repairs; Posterior oblique ligament or joint capsule to tibia; Joint capsule closure to anterior proximal tibia; Medial collateral ligament.

BNS: Fixation in pubic bone for bladder neck suspension using USP #2 Class I nonabsorbable synthetic suture (e.g. polypropylene). A minimum of 2 Anchors should be used in this procedure.

TECHNOLOGICAL CHARACTERSTICS

NONCLINICAL TESTING

MRI Testing using a scanner operating with a static magnetic field was performed on the DePuy Mitek metal implant devices. The test performed, included magnetic field interaction, MRI-related heating, and the presence of artifacts at 3.0 Tesla.

SAFETY AND PERFORMANCE

Results of "Evaluation of Magnetic Field Interactions, Heating, and Artifacts" have demonstrated that the currently marketed DePuy Mitek GII™ Anchors are "MR-conditional".

{2}------------------------------------------------

Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo consists of a stylized eagle with three stripes forming its body and wings. The eagle is enclosed in a circle, with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" arranged around the circumference of the circle.

Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -- WO66-G609 Silver Spring, MD 20993-0002

Mr. Deep Pal Regulatory Affairs Specialist II DePuy Mitek Inc., a johnson and johnson company 325 Paramount Drive RAYNHAM MA 02767

JAN 1 3 2012

Re: K112417

Trade/Device Name: GII™ Anchor Regulation Number: 21 CFR§ 888.3040 Regulation Name: Smooth or threaded metallic bone fixation fastener Regulatory Class: II Product Code: MBI Dated: January 11, 2012 Received: January 12, 2012

Dear Mr. Pal:

We have reviewed your Section 510(k) premarket notification of intent to market the device w oneve and have and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate for about in the May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). and Ocometer for , roo reat the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical

{3}------------------------------------------------

device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to

http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address

http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm.

Sincerely yours,

Benjamin K. Twichell

Benjamin R. Fisher, Ph.D. Director Division of Reproductive, Gastro-Renal, and Urological Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

{4}------------------------------------------------

never stop moving

PRODUCT:	GII™ ANCHOR
SUBMISSION DATE:	AUGUST 22 ND , 20
SUBMISSION TYPE:	TRADITIONAL

ATTACHMENT 2

INDICATIONS FOR USE FORMS

510(k) Number (if known):	" " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " " "Controllation of Concession of

Device Names: GII™ Anchor

Indications for Use:

SHOULDER: Acromio-clavicular; Bankart repair; Biceps tenodesis; Capsule shift/capsulolabral reconstruction; Deltoid repair; Rotator cuff repair; SLAP lesion repair.

ANKLE: Achilles tendon repair/reconstruction; Lateral instability; Medial instability; Midfoot reconstructions.

FOOT: Hallux valgus reconstruction.

WRIST: Scapholunate ligament reconstruction.

HAND: Ulnar or lateral collateral ligament reconstruction.

ELBOW: Biceps tendon reattachment; Tennis elbow repair.

KNEE: Extra capsular reconstruction, ITB tenodesis; Lateral ligament; Patellar ligament and kNew capsuler repairs; Posterior oblique ligament or joint capsule to tibia; Joint capsule closure to anterior proximal tibia; Medial collateral ligament.

BNS: Fixation in pubic bone for bladder neck suspension using USP #2 Class I nonabsorbable synthetic suture (e.g. polypropylene). A minimum of 2 Anchors should be used in this procedure.

Prescription Use (Part 21 CFR 801 Subpart D)

AND/OR

Over-The-Counter Use (21 CFR 807 Subpart C)

2011

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)


(Division Sign-Off)
Division of Reproductive, Gastro-Renal, and Urological Devices

Page 1 of _____

Regulation Number and Section

N/A