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FDA Browser
by
Innolitics
Anesthesiology
Review Panel
Cardiovascular
Review Panel
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Review Panel
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Review Panel
Ear, Nose, Throat
Review Panel
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Review Panel
Hematology
Review Panel
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Review Panel
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Neurology
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Review Panel
Ophthalmic
Review Panel
Diagnostic Devices
CFR Sub-Part
General Hospital and Personal Use Therapeutic Devices
CFR Sub-Part
Miscellaneous
Miscellaneous
Prosthetic Devices
CFR Sub-Part
HPZ
Implant, Eye Sphere
2
Product Code
HQH
Eye, Artificial, Non-Custom
1
Product Code
HQJ
Implant, Absorbable, (Scleral Buckling Methods)
2
Product Code
HQL
Intraocular Lens
3
Product Code
HQM
Keratoprosthesis, Permanent Implant
2
Product Code
K
18
2986
Boston Keratoprosthesis, Type I Lucia
2
Cleared 510(K)
K
12
1203
BOSTON KERATOPROSTHESIS OR BOSTON KPRO
2
Cleared 510(K)
K
01
3756
ALPHACOR; ALPHACOR-A (FOR AHAKIC EYES); ALPHACOR-P (FOR PHAKIC OR PSEUDOPHAKIC EYES)
2
Cleared 510(K)
K
91
5062
DOHLMAN DOANE KERATOPROTHESIS
2
Cleared 510(K)
HQN
Conformer, Ophthalmic
2
Product Code
HQT
Shell, Scleral
2
Product Code
HQW
Clip, Tantalum, Ophthalmic
2
Product Code
HQX
Implant, Orbital, Extra-Ocular
2
Product Code
KYF
Implant, Eye Valve
2
Product Code
MFK
Lens, Multifocal Intraocular
3
Product Code
MJP
Lens, Intraocular, Toric Optics
3
Product Code
MLP
Keratoprosthesis, Temporary Implant, Surgical Use
2
Product Code
MQU
Ocular Peg
2
Product Code
MTZ
Wrap, Implant, Orbital
2
Product Code
NAA
Lens, Intraocular, Accommodative
3
Product Code
NCK
Button, Iris, Eye, Artificial
1
Product Code
NFM
Expander, Tissue, Orbital
2
Product Code
NIZ
Lens, Iris Reconstruction
3
Product Code
NQB
Conformer, Ophthalmic, Biological Tissue
2
Product Code
NXM
Prosthesis, Eyelid Spacer/Graft, Biologic
2
Product Code
POE
Extended Depth Of Focus Intraocular Lens
3
Product Code
PUF
Ocular Peg, Exempt
2
Product Code
PZK
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
3
Product Code
QCB
Phakic Toric Intraocular Lens
3
Product Code
Surgical Devices
CFR Sub-Part
Therapeutic Devices
CFR Sub-Part
Orthopedic
Review Panel
Pathology
Review Panel
Physical Medicine
Review Panel
Radiology
Review Panel
General and Plastic Surgery
Review Panel
Toxicology
Review Panel
Medical Genetics
Review Panel
Unknown
Review Panel
Last synced on 26 May 2023 at 11:04 pm
OP
/
prosthetic-devices
/
HQM
/
K121203
View Source
BOSTON KERATOPROSTHESIS OR BOSTON KPRO
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121203
510(k) Type
Traditional
Applicant
MASSACHUSETTS EYE & EAR INFIRMARY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2013
Days to Decision
385 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
Ophthalmic
Diagnostic Devices
General Hospital and Personal Use Therapeutic Devices
Miscellaneous
Prosthetic Devices
HPZ
Implant, Eye Sphere
HQH
Eye, Artificial, Non-Custom
HQJ
Implant, Absorbable, (Scleral Buckling Methods)
HQL
Intraocular Lens
HQM
Keratoprosthesis, Permanent Implant
K
18
2986
Boston Keratoprosthesis, Type I Lucia
K
12
1203
BOSTON KERATOPROSTHESIS OR BOSTON KPRO
K
01
3756
ALPHACOR; ALPHACOR-A (FOR AHAKIC EYES); ALPHACOR-P (FOR PHAKIC OR PSEUDOPHAKIC EYES)
K
91
5062
DOHLMAN DOANE KERATOPROTHESIS
HQN
Conformer, Ophthalmic
HQT
Shell, Scleral
HQW
Clip, Tantalum, Ophthalmic
HQX
Implant, Orbital, Extra-Ocular
KYF
Implant, Eye Valve
MFK
Lens, Multifocal Intraocular
MJP
Lens, Intraocular, Toric Optics
MLP
Keratoprosthesis, Temporary Implant, Surgical Use
MQU
Ocular Peg
MTZ
Wrap, Implant, Orbital
NAA
Lens, Intraocular, Accommodative
NCK
Button, Iris, Eye, Artificial
NFM
Expander, Tissue, Orbital
NIZ
Lens, Iris Reconstruction
NQB
Conformer, Ophthalmic, Biological Tissue
NXM
Prosthesis, Eyelid Spacer/Graft, Biologic
POE
Extended Depth Of Focus Intraocular Lens
PUF
Ocular Peg, Exempt
PZK
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
QCB
Phakic Toric Intraocular Lens
Surgical Devices
Therapeutic Devices
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
OP
/
prosthetic-devices
/
HQM
/
K121203
View Source
BOSTON KERATOPROSTHESIS OR BOSTON KPRO
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121203
510(k) Type
Traditional
Applicant
MASSACHUSETTS EYE & EAR INFIRMARY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2013
Days to Decision
385 days
Submission Type
Summary