71927790

GUDID 00885556045305

SYNERGY CALCAR STRESSING STEM HIGH OFFSET SZ 16

Smith & Nephew, Inc.

Press-fit femoral stem prosthesis

• Primary Device ID: 00885556045305
• NIH Device Record Key: 6840754d-eef4-4ba3-82f9-969332d10ace
• Commercial Distribution Discontinuation: 2017-07-10
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 71927790
• Catalog Number: 71927790
• Company DUNS: 109903521
• Company Name: Smith & Nephew, 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: true
• 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)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556045305 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K963509

FDA Product Code

• LPH: PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-08-29

Devices Manufactured by Smith & Nephew, Inc.

• 00885556901687 - Q-FIX: 2024-10-14 Q-FIX KNOTLESS ALL-SUTURE ANCHOR 1.8MM WITH ONE ULTRABRAID SUTURE BLUE
• 00885556900567 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 29MM
• 00885556900574 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 32MM
• 00885556900581 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 35MM
• 00885556900598 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 38MM
• 00885556900604 - LEGION/GII: 2024-09-18 PATELLA CAPTURE ROUND/OVAL 41MM
• 00885556900611 - LEGION/GII: 2024-09-18 PATELLA CLAMP ATTACHMENT
• 00885556900628 - LEGION/GII: 2024-09-18 PATELLA SECONDARY SCREW CLAMP