SR™ MCP

GUDID 00886385021041

SR MCP, IMPLANT, SIZE SMALL

Stryker Trauma SA

Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece Metacarpophalangeal joint prosthesis, one-piece
Primary Device ID00886385021041
NIH Device Record Key546e2e55-8027-4e24-8697-dfdaed1d9ec4
Commercial Distribution StatusIn Commercial Distribution
Brand NameSR™ MCP
Version Model Number5800-SM00
Company DUNS481999654
Company NameStryker Trauma SA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness

Device Identifiers

Device Issuing AgencyDevice ID
GS100886385021041 [Primary]

FDA Product Code

MPKSemi-Constrained Metal/Polymer Finger Joint Prosthesis

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-10-07
Device Publish Date2017-06-27

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00886385021102SR MCP, IMPLANT, SIZE X-SMALL
00886385021072SR MCP, IMPLANT, SIZE X-LARGE
00886385021041SR MCP, IMPLANT, SIZE SMALL
00886385021010SR MCP, IMPLANT, SIZE MEDIUM
00886385020983SR MCP, IMPLANT, SIZE LARGE
00886385020976S.R. MCP INSTRUMENT SET, PHALANGEAL IMPACTOR
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00886385020952S.R. MCP AWL ASSEMBLY, SIZE .062
00886385020945S.R. MCP PHALANGEAL BROACH ASSEMBLY, XL
00886385020938S.R. MCP PHALANGEAL BROACH ASSEMBLY, LG
00886385020921S.R. MCP PHALANGEAL BROACH ASSEMBLY, MD
00886385020914S.R. MCP PHALANGEAL BROACH ASSEMBLY, SM
00886385020907S.R. MCP PHALANGEAL BROACH ASSEMBLY, XS
00886385020891S.R. MCP METACARPAL BROACH, SIZE XL
00886385020884S.R. MCP METACARPAL BROACH, SIZE LG
00886385020877S.R. MCP METACARPAL BROACH, SIZE MD
00886385020860S.R. MCP METACARPAL BROACH, SIZE SM
00886385020853S.R. MCP METACARPAL BROACH, SIZE XS
00886385020846S.R. MCP PHALANGEAL TRIAL, SIZE XL
00886385020839S.R. MCP PHALANGEAL TRIAL, SIZE LG
00886385020822S.R. MCP PHALANGEAL TRIAL, SIZE MD
00886385020815S.R. MCP PHALANGEAL TRIAL, SIZE SM
00886385020808S.R. MCP PHALANGEAL TRIAL, SIZE XS
00886385020792S.R. MCP METACARPAL TRIAL, SIZE XL
00886385020785S.R. MCP METACARPAL TRIAL, SIZE LG
00886385020778S.R. MCP METACARPAL TRIAL, SIZE MD
00886385020761S.R. MCP METACARPAL TRIAL, SIZE SM
00886385020754S.R. MCP METACARPAL TRIAL, SIZE XS
00886385020747Nipple Mat for SR MCP Tray
00886385020730S.R. MCP STERILIZATION TRAY BOTTOM
00886385020723S.R. MCP STERILIZATION TRAY LID
00886385020716S.R. MCP TRIAL EXTRACTOR
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