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Innolitics
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OTO
Mesh, Surgical, Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed
2
Product Code
PAJ
Mesh, Surgical, Non-Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed
2
Product Code
K
05
1190
XENFORM SOFT TISSUE REPAIR MATRIX
2
Cleared 510(K)
K
00
2233
BVI SLING
2
Cleared 510(K)
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Last synced on 26 May 2023 at 11:04 pm
OB
/
prosthetic-devices
/
PAJ
/
K002233
View Source
BVI SLING
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002233
510(k) Type
Traditional
Applicant
BIO-VASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/2000
Days to Decision
81 days
Submission Type
Summary
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Neurology
Obstetrical and Gynecological
Assisted Reproduction Devices
Cardiovascular Monitoring Devices
Cardiovascular Prosthetic Devices
Clinical Chemistry Test Systems
Diagnostic Devices
Miscellaneous
Obstetrical and Gynecological Diagnostic Devices
Obstetrical and Gynecological Monitoring Devices
Obstetrical and Gynecological Prosthetic Devices
Obstetrical and Gynecological Surgical Devices
Obstetrical and Gynecological Therapeutic Devices
Physical Medicine Prosthetic Devices
Prosthetic Devices
OTO
Mesh, Surgical, Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed
PAJ
Mesh, Surgical, Non-Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed
K
05
1190
XENFORM SOFT TISSUE REPAIR MATRIX
K
00
2233
BVI SLING
Therapeutic Devices
Ophthalmic
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
OB
/
prosthetic-devices
/
PAJ
/
K002233
View Source
BVI SLING
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002233
510(k) Type
Traditional
Applicant
BIO-VASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/13/2000
Days to Decision
81 days
Submission Type
Summary