510(k) K780579
- Device
- SUBCUPASS TUNNELING TOOL
- Applicant
- MEDTRONIC VASCULAR
- 510(k) number
- K780579
- Product code
- HAO
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1978-05-19
- Date received
- 1978-04-10
- Regulation
- 882.4535
- Classification name
- Instrument, Surgical, Non-powered
- Medical specialty
- Neurology
- Review panel
- Neurology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 4221 Richmond Rd., NW Walker MI US 49534 49534
FDA Registration Numbers#
- 3008911114
- 3014334038
- 9613073
- 3036795921
- 3035708926
- 9680519
- 1219619
- 3011547624
- 3014967149
- 1220724
- 9611502
- 1820334
- 1935627
- 3007507973
- 1220477
- 3004215117
- 1421879
- 3004024955
- 3045522387
- 3003923579
- 8043895
- 8010155
- 9611827
- 3009865268
- 9615005
- 3002807295
- 3007666314
- 2027754
- 3012833053
- 3003435550
- 3002834291
- 8010877
- 3012222873
- 3003418325
- 3010699884
- 8010372
- 1926681
- 3015425095
- 3006984710
- 3005528784
- 9611262
- 8010386
- 9612075
- 3005061536
- 3033536312
- 1421101
- 8040278
- 3005619998
- 3011371465
- 9610612
- 8010405
- 1054811
- 1416891
- 1219653
- 9614062
- 8010168
- 3012507533
- 1928237
- 3010202439
- 3013784566
- 3008770252
- 1056350
- 1057946
- 9614084
- 1061124
- 3006546082
- 3002807090
- 3012226300
- 3009822485
- 3005083075
- 9611579
- 1211566
- 8010591
- 3003696170
- 3008338766
- 8010177
- 3018783415
- 1223656
- 3015546200
- 2182207
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code HAO #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K220920 | Matreneu Percutaneous Balloon Compression Kit | Shenzhen Shineyard Medical Device Co. , Ltd. | 2022-09-07 |
| K940973 | MULLAN GANGLION MICROCOMPRESSION SET | Cook, Inc. | 1995-09-29 |
| K951492 | RIB RESECTOR | United States Surgical, A Division of Tyco Healthc | 1995-05-18 |
| K943115 | AUTO SUTURE PITUITARY SPINAL RONGEUR | United States Surgical, A Division of Tyco Healthc | 1994-07-25 |
| K942967 | AUTO SUTURE SPINAL CURETTE | United States Surgical, A Division of Tyco Healthc | 1994-07-20 |
| K942968 | AUTO SUTURE SPINAL OSTEOTOME | United States Surgical, A Division of Tyco Healthc | 1994-07-20 |
| K942969 | AUTO SUTURE SPINAL NERVE HOOK | United States Surgical, A Division of Tyco Healthc | 1994-07-20 |
| K942970 | AUTO SUTURE SPINAL ELEVATOR | United States Surgical, A Division of Tyco Healthc | 1994-07-20 |
| K942971 | AUTO SUTURE SPINAL DISSECTOR | United States Surgical, A Division of Tyco Healthc | 1994-07-20 |
| K923723 | SILICONE BRAIN SPATULA SET | Redmond Neurosurgical, Inc. | 1992-08-12 |
| K910225 | BONE PAD REMOVER | Acra Cut, Inc. | 1991-02-12 |
| K910226 | DURAL DISSECTORS | Acra Cut, Inc. | 1991-02-12 |
| K902850 | ZEPPELIN INSTRUMENTS | Ruggles Corp. | 1990-07-18 |
| K892546 | TAYLOR SPINAL RETRACTOR | Zinnanti Surgical Instruments, Inc. | 1989-05-11 |
| K882422 | DISPOSABLE ARACHNOID KNIFE | Microbio-Medics, Inc. | 1988-09-06 |
Legacy Summary#
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FDA Review#
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