DEVICE: PHASOR (B775PH53070DTPHKA1S0)

Device Identifier (DI) Information

PHASOR
PH-530-70-DT + PH-K-A1S
In Commercial Distribution
PH-530-70-DT + PH-K-A1S
PHASOR HEALTH LLC
B775PH53070DTPHKA1S0
HIBCC
June 07, 2121
1
111926675 *Terms of Use
Phasor Drill, 5.30-mm diameter, with Drill stop extension, Tapered, plus Kit (version A1) with stapler
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Device Characteristics

MR Unsafe
No
No
Yes
Yes
No
Yes
No
No

GMDN

[?]

GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.

GMDN Term Code GMDN Term Name GMDN Term Definition GMDN Term Status [?] Implantable?
46275 Craniotomy power tool system, battery-powered, single-use
A dedicated battery-powered assembly of devices intended to be used to remove circular sections of the skull vault (calvarium) to provide access to the interior for diagnosis (e.g., the insertion of a neuroscope), or treatments [e.g., to alleviate intracranial pressure (ICP)]; it may also be used for the removal of a bone flap for brain surgery. It typically consists of a handpiece containing a motor (engine), a battery-pack, an attachment with a clutch system that disengages the cutting tool when the inner table has been penetrated preventing injury to the brain, and an exchangeable rotating cutting tool (e.g., a cranial drill bit, bur, trephine or perforator). This is a single-use device.
Obsolete false
44064 Neurosurgical procedure kit, medicated
A collection of various sterile neurosurgical instruments, dressings, pharmaceuticals, and the necessary materials used to perform a neurosurgical procedure. This is a single-use device.
Active false
35884 Skin stapler/staple, non-bioabsorbable
A hand-held manual, surgical instrument preloaded with non-bioabsorbable skin staples designed to apply the staples to approximate the free skin edges of an incision or wound. The staples (which may be clip-like) are made of metal [e.g., stainless steel or titanium (Ti)] and intended to be removed once the wound has sufficiently healed. This is a single-use device.
Active false
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FDA Product Code

[?]
Product Code Product Code Name
HBE Drills, Burrs, Trephines & Accessories (Simple, Powered)
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
K161704 000
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Sterilization

Yes
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

[?]
Storage and Handling
No storage/handling found
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Clinically Relevant Size

[?]
Size Type Text
No Device Sizes
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Device Record Status

7fed6d55-05d4-4a61-b76b-1d3dcee5f6c8
March 07, 2022
2
June 07, 2021
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Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]
Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
No Package DIs found
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Secondary DI

[?]
Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
Yes
Yes
No CLOSE

Customer Contact

[?]
No Customer Contact currently defined
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