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Subpart B—Diagnostic Devices
CFR Sub-Part
Subpart D—Prosthetic Devices
CFR Sub-Part
Subpart E—Neurological Surgical Devices
CFR Sub-Part
OSF
Patient Specific Manual Orthopedic Stereotaxic System
2
Product Code
OJP
Orthopedic Computer Controlled Surgical System
2
Product Code
K
15
0741
TSolution One w/ACG surgical System
2
Cleared 510(K)
K
14
0585
CTC TCAT(R)-TPLAN(R) SURGICAL SYSTEM
2
Cleared 510(K)
K
14
0038
DIGIMATCH ORTHODOC ROBODOC ENCORE SURGICAL SYSTEM
2
Cleared 510(K)
K
07
2629
DIGIMATCH ROBODOC SURGICAL SYSTEM
2
Cleared 510(K)
OLO
Orthopedic Stereotaxic Instrument
2
Product Code
ONN
Intraoperative Orthopedic Joint Assessment Aid
2
Product Code
OSE
Patient Specific Manual Navigation System
2
Product Code
SBF
Orthopedic Augmented Reality
2
Product Code
Subpart E—Surgical Devices
CFR Sub-Part
Pathology
Review Panel
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Unknown
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Last synced on 16 May 2025 at 11:05 pm
OR
/
subpart-e—neurological-surgical-devices
/
OJP
/
K150741
View Source
TSolution One w/ACG surgical System
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150741
510(k) Type
Traditional
Applicant
THINK SURGICAL INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2015
Days to Decision
213 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
Orthopedic
Miscellaneous
Subpart B—Diagnostic Devices
Subpart D—Prosthetic Devices
Subpart E—Neurological Surgical Devices
OSF
Patient Specific Manual Orthopedic Stereotaxic System
OJP
Orthopedic Computer Controlled Surgical System
K
15
0741
TSolution One w/ACG surgical System
K
14
0585
CTC TCAT(R)-TPLAN(R) SURGICAL SYSTEM
K
14
0038
DIGIMATCH ORTHODOC ROBODOC ENCORE SURGICAL SYSTEM
K
07
2629
DIGIMATCH ROBODOC SURGICAL SYSTEM
OLO
Orthopedic Stereotaxic Instrument
ONN
Intraoperative Orthopedic Joint Assessment Aid
OSE
Patient Specific Manual Navigation System
SBF
Orthopedic Augmented Reality
Subpart E—Surgical Devices
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
OR
/
subpart-e—neurological-surgical-devices
/
OJP
/
K150741
View Source
TSolution One w/ACG surgical System
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150741
510(k) Type
Traditional
Applicant
THINK SURGICAL INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/22/2015
Days to Decision
213 days
Submission Type
Summary