N/A 00-2329-014-18

GUDID 00889024049888

Zimmer, Inc.

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Primary Device ID	00889024049888
NIH Device Record Key	8e5b8958-e71b-4690-b3a1-8ef209dc17f7
Commercial Distribution Status	In Commercial Distribution
Brand Name	N/A
Version Model Number	00-2329-014-18
Catalog Number	00-2329-014-18
Company DUNS	056038268
Company Name	Zimmer, Inc.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com
Phone	+1(800)348-2759
Email	zimmer.consumerrelations@zimmerbiomet.com

Device Dimensions

Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter
Device Size Text, specify	0
Length	14 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024049888 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K133246

FDA Product Code

HWC	Screw, fixation, bone